@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_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/> .
@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/v4.0.0/void/> .

dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_head {
  this: np:hasAssertion dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_assertion;
    np:hasProvenance dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_provenance;
    np:hasPublicationInfo dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_assertion a np:Assertion .
  
  dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_provenance a np:Provenance .
  
  dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_assertion {
  miriam-gene:2776 a ncit:C16612 .
  
  lld:C0042162 a ncit:C7057 .
  
  dgn-gda:DGNf753f97c3c7dc631d2c56e7e3bacc275 sio:SIO_000628 miriam-gene:2776, lld:C0042162;
    a sio:SIO_001122 .
}

dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_provenance {
  dgn-np:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_assertion dcterms:description
      "[The GNAQ209 mutation rate in uveal melanoma in this study is in line with the rate in other reports. The finding of the same genotype in the primary tumors and their metastases suggests that mutation in GNAQ is an early event in uveal melanoma tumorigenes]. 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:20631239;
    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:NP181528.RAP4GJnfdXemWwEarvlzztGXd7kip3EXrzryu7fHpav_E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:09+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}