@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE> .
@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:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_head {
  this: np:hasAssertion dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_assertion;
    np:hasProvenance dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_provenance;
    np:hasPublicationInfo dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_assertion a np:Assertion .
  
  dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_provenance a np:Provenance .
  
  dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_assertion {
  miriam-gene:7167 a ncit:C16612 .
  
  lld:C0025517 a ncit:C7057 .
  
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    a sio:SIO_001121 .
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dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_provenance {
  dgn-np:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_assertion dcterms:description
      "[These novel results confirm the existence of a transport mechanism which permits transfer of active TPI from K562 cells to deficient cells, and may have important implications for developing different therapeutic approaches for TPI deficiency and other metabolic disorders of glycolysis.]. 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:9125215;
    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:NP683742.RAYeU32a_mM5BCUawqLlo8lNJeZc55aDrET3PP4bIKXHE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:55+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}