@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w> .
@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:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_head {
  this: np:hasAssertion dgn-np:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_assertion;
    np:hasProvenance dgn-np:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_provenance;
    np:hasPublicationInfo dgn-np:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_assertion a np:Assertion .
  
  dgn-np:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_provenance a np:Provenance .
  
  dgn-np:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_assertion {
  miriam-gene:5265 a ncit:C16612 .
  
  lld:C0023890 a ncit:C7057 .
  
  dgn-gda:DGNca1d7e3342cab0e07e19d68c45efaedb sio:SIO_000628 miriam-gene:5265, lld:C0023890;
    a sio:SIO_001121 .
}

dgn-np:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_provenance {
  dgn-np:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_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-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:NP461341.RABFqgtCZUJM3yK-rfSgAM6GOIPr86vg1Ylo0CqxwNe8w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:34+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" .
}