@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4> .
@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:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_head {
  this: np:hasAssertion dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_assertion;
    np:hasProvenance dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_provenance;
    np:hasPublicationInfo dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_assertion a np:Assertion .
  
  dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_provenance a np:Provenance .
  
  dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0042373 a ncit:C7057 .
  
  dgn-gda:DGN37e8a43aa026f3843bc587ed28518e78 sio:SIO_000628 miriam-gene:4524, lld:C0042373;
    a sio:SIO_001121 .
}

dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_provenance {
  dgn-np:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_assertion dcterms:description
      "[These data suggest that in selected patients homozygosity for the MTHFR mutation increases the risk of both arterial and venous thromboses and that differences in selection criteria for the patient group may be responsible in part for the controversial association of the MTHFR mutation and vascular disease.]. 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:10477457;
    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:NP262312.RAmcDfyPr5FkelA0P1rKcKe77dM1uw-QS3GrmRcUxtWB4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:45+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" .
}