@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg> .
@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:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_head {
  this: np:hasAssertion dgn-np:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_assertion ;
    np:hasProvenance dgn-np:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_provenance ;
    np:hasPublicationInfo dgn-np:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_assertion a np:Assertion .
  dgn-np:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_provenance a np:Provenance .
  dgn-np:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_assertion {
  miriam-gene:2776 a ncit:C16612 .
  lld:C0206736 a ncit:C7057 .
  dgn-gda:DGN3b2d30096435b86f9129c0c20a1f7741 sio:SIO_000628 miriam-gene:2776 , lld:C0206736 ;
    a sio:SIO_001121 .
}
dgn-np:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_provenance {
  dgn-np:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_assertion dcterms:description "[The presence of GNAQ mutations in the amelanotic/hypomelanotic blue nevus indicates that mechanisms underlying pigment homeostasis in this variant appear to be similar to those of its melanotic counterparts, although it is not clear why activation of the q class of the G-protein α subunit should cause an abundance of dermal pigment in one variant and not in another.]. 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:21056896 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP317877.RAMwvPG7aCoyy0gGLCMC-OyjUTXHRNwUjDuplahb1h-Dg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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" .
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}