@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_head {
  this: np:hasAssertion dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_assertion ;
    np:hasProvenance dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_provenance ;
    np:hasPublicationInfo dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_assertion a np:Assertion .
  dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_provenance a np:Provenance .
  dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_assertion {
  miriam-gene:50840 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
  dgn-gda:DGN52f25967a79ccb4e4f7c03a553698833 sio:SIO_000628 miriam-gene:50840 , lld:C1527249 ;
    a sio:SIO_001122 .
}
dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_provenance {
  dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_assertion dcterms:description "[In conclusion we can confidently exclude a major role for common polymorphisms of the TAS2R14 gene in colorectal cancer risk in this population, although in this report we had insufficient statistical power to completely exclude the possibility that rare variants of the TAS2R14 might be involved in colorectal cancer risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:20534144 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP91015.RAyVHhdZwV__w3OXjQXNNV7eIu9upcFnv4xjjVlNjyV-E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:45+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}