@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM> .
@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:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_head {
  this: np:hasAssertion dgn-np:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_assertion;
    np:hasProvenance dgn-np:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_provenance;
    np:hasPublicationInfo dgn-np:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_assertion a np:Assertion .
  
  dgn-np:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_provenance a np:Provenance .
  
  dgn-np:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_assertion {
  miriam-gene:611 a ncit:C16612 .
  
  lld:C0023895 a ncit:C7057 .
  
  dgn-gda:DGN1395170dcc4990fde404c4fd3a38f1b8 sio:SIO_000628 miriam-gene:611, lld:C0023895;
    a sio:SIO_001121 .
}

dgn-np:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_provenance {
  dgn-np:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_assertion dcterms:description
      "[Thus, the aim of this study was to determine the incidence of BCP and precore HBV mutants and their relationship with HBV genotype and different stages of HBV related liver disease in North Indian patients.]. 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:20043209;
    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:NP363155.RANlo9vy4jETWT-mV8ogGU2wB-HfdYBqTHbL2HPXScQfM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:32+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" .
}