@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg> .
@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:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_head {
  this: np:hasAssertion dgn-np:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_assertion;
    np:hasProvenance dgn-np:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_provenance;
    np:hasPublicationInfo dgn-np:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_assertion a np:Assertion .
  
  dgn-np:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_provenance a np:Provenance .
  
  dgn-np:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_assertion {
  miriam-gene:7037 a ncit:C16612 .
  
  lld:C0025286 a ncit:C7057 .
  
  dgn-gda:DGN6b16e75b04492946120c6155aa21acd0 sio:SIO_000628 miriam-gene:7037, lld:C0025286;
    a sio:SIO_001121 .
}

dgn-np:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_provenance {
  dgn-np:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_assertion dcterms:description
      "[Notable findings include high expression of transferrin receptor 1 in the hippocampus and medulla oblongata compared to other brain regions, low expression of HFE in normal brain with elevated HFE expression in meningiomas, and absence of hepcidin mRNA in astrocytoma cell lines despite expression in normal brain and tumor specimens.]. 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:19386095;
    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:NP290138.RAS_yz797OdQ0S6C5FhsP0AE0nzMldNQ8hyrIL1kk2LLg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:45+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" .
}