@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok> .
@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:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_head {
  this: np:hasAssertion dgn-np:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_assertion;
    np:hasProvenance dgn-np:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_provenance;
    np:hasPublicationInfo dgn-np:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_assertion a np:Assertion .
  
  dgn-np:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_provenance a np:Provenance .
  
  dgn-np:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_assertion {
  miriam-gene:4843 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGN490d08ec38a6787e32f2ed3328560ebc sio:SIO_000628 miriam-gene:4843, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_provenance {
  dgn-np:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_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: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:NP596342.RAs-mfPUDGn5CA-9nOi_bflSjnDjrGfXUTw9-SAHbROok130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:16+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" .
}