@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE> .
@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:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_head {
  this: np:hasAssertion dgn-np:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_assertion ;
    np:hasProvenance dgn-np:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_provenance ;
    np:hasPublicationInfo dgn-np:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_assertion a np:Assertion .
  dgn-np:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_provenance a np:Provenance .
  dgn-np:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_assertion {
  miriam-gene:931 a ncit:C16612 .
  lld:C0751955 a ncit:C7057 .
  dgn-gda:DGN458725c6897afabbadda2e7975ba4ffd sio:SIO_000628 miriam-gene:931 , lld:C0751955 ;
    a sio:SIO_001122 .
}
dgn-np:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_provenance {
  dgn-np:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_assertion dcterms:description "[ Gene mutations as CBS 844ins 68, MS A2756G and MTHFR C677T may not be independent risk factors for ischemic cardiovascular and cerebrovascular disease in Southern Chinese Han population. The prevalences of CBS 844ins 68 and MS A2756G may vary with differ]. 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:11758232 ;
    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:NP72319.RAqOHNjvwqFLGOD5xiGEDjIs1s4T1jPA-IdNDpemB5bgE130_publicationInfo {
  this: dcterms:created "2016-05-13T12:42:21+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" .
}