@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw> .
@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 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:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_head {
  this: np:hasAssertion dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_assertion;
    np:hasProvenance dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_provenance;
    np:hasPublicationInfo dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_assertion a np:Assertion .
  
  dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_provenance a np:Provenance .
  
  dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_assertion {
  miriam-gene:7508 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGNe97af5dade617c747630a2e2e7326e2c sio:SIO_000628 miriam-gene:7508, lld:C0025202;
    a sio:SIO_001122 .
}

dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_provenance {
  dgn-np:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_assertion dct:description
      "[We found no association of the homozygous 1580A, 1601C, 2166A, and 3507G genotypes with increased risks of melanoma. Exploratory analyses of subgroups of melanoma patients compared to all controls indicated no association of these genotypes with increased risks for development of multiple primary melanomas (n=28), a negative family history for melanoma (n=277), melanomas in individuals with a low number of nevi (n=273), melanomas in individuals older than 55 years (n=142), and melanomas thicker than 1 mm (n=126).]. 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:15494739;
    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:NP59340.RA6pWMtLeRH1bu0soGugwox0Z4Qnr1Qo5co5gCSmrE9yw130_publicationInfo {
  this: dct:created "2014-10-02T12:32:28+02:00"^^xsd:dateTime;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dct:rightsHolder dgn-void:IBIGroup;
    dct:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
      orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
    pav:createdBy orcid:0000-0003-0169-8159;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}