@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .
dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_head {
  this: np:hasAssertion dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_assertion ;
    np:hasProvenance dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_provenance ;
    np:hasPublicationInfo dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_assertion a np:Assertion .
  dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_provenance a np:Provenance .
  dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_assertion {
  miriam-gene:4157 a ncit:C16612 .
  lld:C0037286 a ncit:C7057 .
  dgn-gda:DGN7d84aa92a7d1bcfc981ce356d4137f80 sio:SIO_000628 miriam-gene:4157 , lld:C0037286 ;
    a sio:SIO_001122 .
}
dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_provenance {
  dgn-np:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_assertion dcterms:description "[Results show that MC1R variants, hair color, and number of nevi were jointly associated with melanoma risk in CDKN2A mutation carriers. This joint association may have important consequences for risk assessments in familial settings.]. 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:20876876 ;
    prov:wasDerivedFrom dgn-void:gad-20150221 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP93404.RAXtfzCojH4AYZsBruu9c-11GouMzCUAYckmsZZMEGURk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:31+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:disgenetv3.0rdf ;
    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 "v3.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}