@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg> .
@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:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_head {
  this: np:hasAssertion dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_assertion ;
    np:hasProvenance dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_provenance ;
    np:hasPublicationInfo dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_assertion a np:Assertion .
  dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_provenance a np:Provenance .
  dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_assertion {
  miriam-gene:10855 a ncit:C16612 .
  lld:C0018133 a ncit:C7057 .
  dgn-gda:DGNa26f03705b73ecd3b1c6ff24120e56f6 sio:SIO_000628 miriam-gene:10855 , lld:C0018133 ;
    a sio:SIO_001121 .
}
dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_provenance {
  dgn-np:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_assertion dcterms:description "[Identification and characterization of a human heparanase splice variant (T5) devoid of enzymatic activity and endowed with protumorigenic characteristics, elucidation of cross-talk between heparanase and other extracellular matrix-degrading enzymes, and identification of single nucleotide polymorphism associated with heparanase expression and increased risk of graft versus host disease add other layers of complexity to heparanase function in health and disease.]. 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:20840586 ;
    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:NP402998.RAH-1KVzr4nyasjSuuFFT_ZhkFGynCesKUmhVF-6eOhEg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:00+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" .
}