@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4> .
@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:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_head {
  this: np:hasAssertion dgn-np:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_assertion ;
    np:hasProvenance dgn-np:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_provenance ;
    np:hasPublicationInfo dgn-np:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_assertion a np:Assertion .
  dgn-np:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_provenance a np:Provenance .
  dgn-np:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_assertion {
  miriam-gene:54984 a ncit:C16612 .
  lld:C0019163 a ncit:C7057 .
  dgn-gda:DGN02bb8288cb80ce6f22878f66bad8abf8 sio:SIO_000628 miriam-gene:54984 , lld:C0019163 ;
    a sio:SIO_001121 .
}
dgn-np:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_provenance {
  dgn-np:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_assertion dcterms:description "[Interestingly, LOH was identified only in HCC samples with hepatitis B virus (HBV) infection and the frequency of LOH was not statistically related with histologic grade and clinical stage, suggesting that allelic loss of the LPTS gene may occur as an early event in the development of HCC, especially in the cases with HBV infection.]. 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:11867205 ;
    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:NP817236.RAoH-dAiEBvAok45OHDyDA_lkcCo8eNi4kpbvdetmC9U4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:20+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" .
}