@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk> .
@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:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_head {
  this: np:hasAssertion dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_assertion;
    np:hasProvenance dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_provenance;
    np:hasPublicationInfo dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_assertion a np:Assertion .
  
  dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_provenance a np:Provenance .
  
  dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_assertion {
  miriam-gene:182 a ncit:C16612 .
  
  lld:C0015544 a ncit:C7057 .
  
  dgn-gda:DGNb07236d1b00e3be122725bbeb328bc62 sio:SIO_000628 miriam-gene:182, lld:C0015544;
    a sio:SIO_001121 .
}

dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_provenance {
  dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_assertion dcterms:description
      "[Arteriohepatic dysplasia (AHD, Alagille's syndrome) is presumed to be one of the six known familial intrahepatic cholestatic syndromes, all of which present with neonatal jaundice or failure to thrive, or both.]. 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:7254780;
    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:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:34+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" .
}