@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I> .
@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:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_head {
  this: np:hasAssertion dgn-np:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_assertion;
    np:hasProvenance dgn-np:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_provenance;
    np:hasPublicationInfo dgn-np:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_assertion a np:Assertion .
  
  dgn-np:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_provenance a np:Provenance .
  
  dgn-np:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0747845 a ncit:C7057 .
  
  dgn-gda:DGN9ef938999efb83cd966f04f7390cd189 sio:SIO_000628 miriam-gene:4524, lld:C0747845;
    a sio:SIO_001121 .
}

dgn-np:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_provenance {
  dgn-np:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_assertion dcterms:description
      "[With the present study we can show for the first time that the embryonal MTHFR 677TT genotype is significantly associated with the development of structural congenital heart malformations during early pregnancy.]. 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:11470464;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP575980.RAHz0VAhFZzHS84HlSHZ7o1H5C4e4Zwx2scQC9d5DAn0I130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:23+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" .
}