@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s> .
@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:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_head {
  this: np:hasAssertion dgn-np:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_assertion;
    np:hasProvenance dgn-np:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_provenance;
    np:hasPublicationInfo dgn-np:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_assertion a np:Assertion .
  
  dgn-np:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_provenance a np:Provenance .
  
  dgn-np:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_assertion {
  miriam-gene:2247 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
  dgn-gda:DGN559c4ce77a55b1fe7d048f4c9ef5c040 sio:SIO_000628 miriam-gene:2247, lld:C0025202;
    a sio:SIO_001121 .
}

dgn-np:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_provenance {
  dgn-np:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_assertion dcterms:description
      "[1F6 human melanoma xenografts overexpressing either the 18 kD (18kD) form or all (ALL) forms of human basic fibroblast growth factor (bFGF) demonstrate an abundant number of microvessels and accelerated growth.]. 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:19478386;
    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:NP335524.RApU3v0HR9QxLyowq35ijsHa4Z0QT4MXYjOK2QlUtga1s130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:17+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" .
}