@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk> .
@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:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_head {
  this: np:hasAssertion dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_assertion;
    np:hasProvenance dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_provenance;
    np:hasPublicationInfo dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_assertion a np:Assertion .
  
  dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_provenance a np:Provenance .
  
  dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_assertion {
  miriam-gene:7422 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGN0cd010da5ed41c3da843a8354e6d9d4e sio:SIO_000628 miriam-gene:7422, lld:C0002736;
    a sio:SIO_001121 .
}

dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_provenance {
  dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_assertion dcterms:description
      "[Although VEGF gene expression is mainly stimulated by hypoxia, we have measured lower VEGF levels in cerebrospinal fluid (CSF) from hypoxaemic patients with amyotrophic lateral sclerosis (ALS) than in CSF from normoxaemic patients with ALS.]. 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:16421133;
    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:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}