@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA> .
@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:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_head {
  this: np:hasAssertion dgn-np:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_assertion;
    np:hasProvenance dgn-np:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_provenance;
    np:hasPublicationInfo dgn-np:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_assertion a np:Assertion .
  
  dgn-np:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_provenance a np:Provenance .
  
  dgn-np:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_assertion {
  miriam-gene:4524 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN7ab0fbfec54914919cebb2b843b4c2ed sio:SIO_000628 miriam-gene:4524, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_provenance {
  dgn-np:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_assertion dcterms:description
      "[Whereas our results do not support an association of high enzyme activity and increased risk of colorectal cancer in general, we can not exclude an association of patients with hereditary disease and the MTHFR 1298A --> C variant.]. 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:12618331;
    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:NP243515.RAlC-_nPJILzIZMbTh8mrD3XI5UtjbnMUGnu5H8ffqwxA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:16+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" .
}