@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg> .
@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:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_head {
  this: np:hasAssertion dgn-np:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_assertion;
    np:hasProvenance dgn-np:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_provenance;
    np:hasPublicationInfo dgn-np:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_assertion a np:Assertion .
  
  dgn-np:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_provenance a np:Provenance .
  
  dgn-np:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_assertion {
  miriam-gene:4548 a ncit:C16612 .
  
  lld:C3806347 a ncit:C7057 .
  
  dgn-gda:DGN35c11ff5f300caa19c67471453af9a73 sio:SIO_000628 miriam-gene:4548, lld:C3806347;
    a sio:SIO_001122 .
}

dgn-np:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_provenance {
  dgn-np:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_assertion dcterms:description
      "[In summary, larger and homogeneous study populations are necessary to quantify the small effects of common mutations on homocysteine levels. This may also be the reason that no effects of genetic interactions between two genotypes were observed.]. 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:11592436;
    prov:wasDerivedFrom dgn-void:gad-20150221;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP79671.RAYVnlNI8hRufAO_NSBH5aA0gtrNvRM6OQW6acSFhPFgg130_publicationInfo {
  this: dcterms:created "2015-08-25T14:38:23+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" .
}