@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg> .
@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:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_head {
  this: np:hasAssertion dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_assertion;
    np:hasProvenance dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_provenance;
    np:hasPublicationInfo dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_assertion a np:Assertion .
  
  dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_provenance a np:Provenance .
  
  dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_assertion {
  miriam-gene:10161 a ncit:C16612 .
  
  lld:C0018500 a ncit:C7057 .
  
  dgn-gda:DGN7841f6418ea22663081f6f851d2cc55b sio:SIO_000628 miriam-gene:10161, lld:C0018500;
    a sio:SIO_001121 .
}

dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_provenance {
  dgn-np:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_assertion dcterms:description
      "[Although these findings clearly reveal the involvement of P2RY5 mutations in hereditary hair diseases, the clinical manifestations of P2RY5 mutations have not completely been elucidated because of limited information to date.]. 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:18803659;
    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:NP387634.RA6TKvpNOmExbmF8LvTuL1ggCfPo52rNK1Q03xZPcs4Vg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:51+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" .
}