@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8> .
@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:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_head {
  this: np:hasAssertion dgn-np:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_assertion;
    np:hasProvenance dgn-np:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_provenance;
    np:hasPublicationInfo dgn-np:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_assertion a np:Assertion .
  
  dgn-np:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_provenance a np:Provenance .
  
  dgn-np:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_assertion {
  miriam-gene:1913 a ncit:C16612 .
  
  lld:C0265554 a ncit:C7057 .
  
  dgn-gda:DGN90610db40319f43c63cfa891fa075d3b sio:SIO_000628 miriam-gene:1913, lld:C0265554;
    a sio:SIO_001121 .
}

dgn-np:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_provenance {
  dgn-np:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_assertion dcterms:description
      "[These complex patients included those with single gene disorders in which SHFM has been reported (e.g., ectodermal dysplasia Ectrodactyly Clefting (EEC), tibial aplasia with SHFM, fibular aplasia with SHFM), as well as those with other recognized or unknown patterns of anomalies.]. 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:16673359;
    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:NP704974.RAPyIXbVEFQmbkP7w8X5IAUkyqOt0rLWHRnxXOemOKwe8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:08+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" .
}