@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk> .
@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:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_head {
  this: np:hasAssertion dgn-np:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_assertion;
    np:hasProvenance dgn-np:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_provenance;
    np:hasPublicationInfo dgn-np:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_assertion a np:Assertion .
  
  dgn-np:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_provenance a np:Provenance .
  
  dgn-np:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_assertion {
  miriam-gene:2776 a ncit:C16612 .
  
  lld:C0220633 a ncit:C7057 .
  
  dgn-gda:DGN6f68d2107d0da5af138f243ff1352066 sio:SIO_000628 miriam-gene:2776, lld:C0220633;
    a sio:SIO_001121 .
}

dgn-np:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_provenance {
  dgn-np:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_assertion dcterms:description
      "[However, somatic mutations in either GNAQ or GNA11 are unique to UM tumors and could be used as potential markers to differentiate UM from metastatic CM and act as direct therapeutic targets.]. 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:24697775;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1169891.RAQxAt8w61Feeyggi9b5s2ZoqMW357R1DBGDoTJAIPNJk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:36+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" .
}