@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_head {
  this: np:hasAssertion dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_assertion;
    np:hasProvenance dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_provenance;
    np:hasPublicationInfo dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_assertion a np:Assertion .
  
  dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_provenance a np:Provenance .
  
  dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_assertion {
  miriam-gene:5265 a ncit:C16612 .
  
  lld:C0018995 a ncit:C7057 .
  
  dgn-gda:DGN50485d4cd4d0b1a58bea5a063450b220 sio:SIO_000628 miriam-gene:5265, lld:C0018995;
    a sio:SIO_001122 .
}

dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_provenance {
  dgn-np:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_assertion dcterms:description
      "[The presence of the relatively high frequency of A1AT S and HFE H63D allele carriers in Egyptian cases of HCV liver cirrhosis suggest the necessity to implement routine molecular analysis of these genes for detection of risk genotypes among affected families.]. 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:16802007;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP619796.RA53TpsOwD8wlxP1E1y7GHCYA4A_jdoDaFNoVxF-fgk7g130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:50+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}