@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix ns0: <http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix metadata_def: <http://data.bioontology.org/metadata/def/> .
@prefix metadata: <http://data.bioontology.org/metadata/> .
ns0:aa_variation
rdfs:subClassOf ns0:observed_variation .
ns0:database
owl:disjointWith ns0:observed_variation .
ns0:hasVariantAASequence
rdfs:domain ns0:observed_variation .
ns0:hasVariantAlleleSequence
rdfs:domain ns0:observed_variation .
ns0:hasVariantSequence
rdfs:domain ns0:observed_variation .
ns0:isOneObservedAASequenceIn
rdfs:range ns0:observed_variation .
ns0:isOneObservedAlleleIn
rdfs:range ns0:observed_variation .
ns0:isOneObservedVariantIn
rdfs:range ns0:observed_variation .
ns0:nucleotide_variation
rdfs:subClassOf ns0:observed_variation .
ns0:observed_variation
metadata_def:mappingLoom "observedvariation" ;
metadata_def:mappingSameURI ns0:observed_variation ;
metadata_def:prefLabel "observed_variation" ;
metadata:prefixIRI "SNPO:observed_variation" ;
a owl:Class ;
rdfs:comment """It is the variation (of nucleotides or of residues) observed between the 2 patients (reference sequence and the alternative sequence - if it's possible to talk about a \"reference\") when a genomic variation is described.
Ex: A>C, CT>A, Ser>Thr, etc.""" ;
rdfs:subClassOf owl:Thing ;
owl:disjointWith ns0:sequence, ns0:sequence_position, ns0:variant .
@prefix rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix ns0: <http://www.loria.fr/~coulet/ontology/snpontology/version1.6/snpontology_full.owl#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix metadata_def: <http://data.bioontology.org/metadata/def/> .
@prefix metadata: <http://data.bioontology.org/metadata/> .
ns0:aa_variation
rdfs:subClassOf ns0:observed_variation .
ns0:database
owl:disjointWith ns0:observed_variation .
ns0:hasVariantAASequence
rdfs:domain ns0:observed_variation .
ns0:hasVariantAlleleSequence
rdfs:domain ns0:observed_variation .
ns0:hasVariantSequence
rdfs:domain ns0:observed_variation .
ns0:isOneObservedAASequenceIn
rdfs:range ns0:observed_variation .
ns0:isOneObservedAlleleIn
rdfs:range ns0:observed_variation .
ns0:isOneObservedVariantIn
rdfs:range ns0:observed_variation .
ns0:nucleotide_variation
rdfs:subClassOf ns0:observed_variation .
ns0:observed_variation
metadata_def:mappingLoom "observedvariation" ;
metadata_def:mappingSameURI ns0:observed_variation ;
metadata_def:prefLabel "observed_variation" ;
metadata:prefixIRI "SNPO:observed_variation" ;
a owl:Class ;
rdfs:comment """It is the variation (of nucleotides or of residues) observed between the 2 patients (reference sequence and the alternative sequence - if it's possible to talk about a \"reference\") when a genomic variation is described.
Ex: A>C, CT>A, Ser>Thr, etc.""" ;
rdfs:subClassOf owl:Thing ;
owl:disjointWith ns0:sequence, ns0:sequence_position, ns0:variant .