@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk> .
@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:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_head {
  this: np:hasAssertion dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_assertion;
    np:hasProvenance dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_provenance;
    np:hasPublicationInfo dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_assertion a np:Assertion .
  
  dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_provenance a np:Provenance .
  
  dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_assertion {
  miriam-gene:3077 a ncit:C16612 .
  
  lld:C0524851 a ncit:C7057 .
  
  dgn-gda:DGN33334aa07bbc2aa6559ed1d48f8bde08 sio:SIO_000628 miriam-gene:3077, lld:C0524851;
    a sio:SIO_001121 .
}

dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_provenance {
  dgn-np:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_assertion dcterms:description
      "[Because of the increasing evidence that H63D HFE polymorphism appears in higher frequency in neurodegenerative diseases, we evaluated the neurological consequences of H63D HFE in vivo using mice that carry H67D HFE (homologous to human H63D).]. 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:23429074;
    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:NP343729.RAMThKZhlZV61qoLenNufM9DmjPSRjTZm6jJTlz9_8ifk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:22+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}