@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk> .
@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/v3.0.0/void/> .

dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_head {
  this: np:hasAssertion dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_assertion;
    np:hasProvenance dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_provenance;
    np:hasPublicationInfo dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_assertion a np:Assertion .
  
  dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_provenance a np:Provenance .
  
  dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0034065 a ncit:C7057 .
  
  dgn-gda:DGN3ae0e5f8d2a33aac16e74aa84bee7e15 sio:SIO_000628 miriam-gene:4524, lld:C0034065;
    a sio:SIO_001122 .
}

dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_provenance {
  dgn-np:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_assertion dcterms:description
      "[, coagulant factor V gene G1691A mutation and prothrombin G20210A mutation are very rare, while MTHFR C677T mutation is very common, and all of them are not associated with pulmonary thromboembolism in the Chinese population.]. 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:12165282;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP91453.RAc0xwFeJCQ8c3FZo3YWhfdhxNP3i3CYpfMBh0axz2iXk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:30+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}