@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo> .
@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:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_head {
   this: np:hasAssertion dgn-np:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_assertion ;
    np:hasProvenance dgn-np:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_provenance ;
    np:hasPublicationInfo dgn-np:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_assertion a np:Assertion .
  dgn-np:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_provenance a np:Provenance .
  dgn-np:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_assertion {
   miriam-gene:4548 a ncit:C16612 .
  lld:C1168401 a ncit:C7057 .
  dgn-gda:DGN5511a33fa5ea19b1ceb228e9818e83a1 sio:SIO_000628 miriam-gene:4548 , lld:C1168401 ;
    a sio:SIO_001121 .
}
dgn-np:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_provenance {
   dgn-np:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_assertion dcterms:description "[The association between 203 tag-SNPs (tSNPs) of 15 FMP associated genes (CBS, BHMT, DHFR, FOLR1, FOLR2, FOLR3, MTHFR, MTR, MTRR, MTHFD1, RFC1, SHMT1, SLC19A1, TCN2, and TYMS) and incident HNC was investigated in 23,294 Caucasian female participants of the prospective Women's Genome Health Study.]. 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:23276522 ;
    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:NP698794.RAWU3E_lJskplbxH_0nvcrvz-rLiBMIQA8J3o0glFrUFo130_publicationInfo {
   this: dcterms:created "2014-10-02T12:39:05+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" .
}