@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M> .
@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:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_head {
   this: np:hasAssertion dgn-np:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_assertion ;
    np:hasProvenance dgn-np:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_provenance ;
    np:hasPublicationInfo dgn-np:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_assertion a np:Assertion .
  dgn-np:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_provenance a np:Provenance .
  dgn-np:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_assertion {
   miriam-gene:4524 a ncit:C16612 .
  lld:C0018798 a ncit:C7057 .
  dgn-gda:DGNd1947a057d371d431be19beb703de0cc sio:SIO_000628 miriam-gene:4524 , lld:C0018798 ;
    a sio:SIO_001122 .
}
dgn-np:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_provenance {
   dgn-np:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_assertion dcterms:description "[To observe the association of MTHFR gene C677T locus polymorphism with occurrence of congenital heart defects (CHDs), 21 patients with atrial septal defect (ASD), 35 patients with patent ductus arteriosus (PDA), one patient with both conditions combined, and their biological parents were collected as the case group.]. 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:16373366 ;
    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:NP528168.RAUi0nCvQuxOtI96BPheG38LDQfxxgC91UHfewpp5QR3M130_publicationInfo {
   this: dcterms:created "2016-05-13T12:45:44+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" .
}