@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM> .
@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:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_head {
  this: np:hasAssertion dgn-np:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_assertion;
    np:hasProvenance dgn-np:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_provenance;
    np:hasPublicationInfo dgn-np:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_assertion a np:Assertion .
  
  dgn-np:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_provenance a np:Provenance .
  
  dgn-np:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_assertion {
  miriam-gene:4842 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNc192feadd84c21cee16f9df11bea7ced sio:SIO_000628 miriam-gene:4842, lld:C0025202;
    a sio:SIO_001122 .
}

dgn-np:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_provenance {
  dgn-np:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_assertion dcterms:description
      "[Genetic variants of nNOS, but not iNOS, may be biomarkers for susceptibility to CM, and the risk of CM associated with sunburns and moles may be modulated by nNOS variant genotypes.]. 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:17328085;
    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:NP67498.RAe1o7XLGQw4aIZRa5_nwfSY8qVt5qVN7JVub07GSNTBM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}