@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_head {
  this: np:hasAssertion dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_assertion;
    np:hasProvenance dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_provenance;
    np:hasPublicationInfo dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_assertion a np:Assertion .
  
  dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_provenance a np:Provenance .
  
  dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0810364 a ncit:C7057 .
  
  dgn-gda:DGNfd197eb1458e67e368c639f2b5dcebce sio:SIO_000628 miriam-gene:4524, lld:C0810364;
    a sio:SIO_001121 .
}

dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_provenance {
  dgn-np:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_assertion dcterms:description
      "[Because of MTHFR's involvement with folate metabolism and evidence that maternal use of a multivitamin with folic acid in early pregnancy reduces risk for cleft lip with or without cleft palate (CLP), we hypothesized that infants homozygous for the C677T genotype would be at increased risk for CLP because of lower MTHFR enzymatic activity.]. 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:9843036;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP377886.RAI33an_RfPyX_lqfLX8J6tswJFjzyXAZH0MhipOhV0Xk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:41+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}