@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E> .
@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/v4.0.0/void/> .

dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_head {
  this: np:hasAssertion dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_assertion;
    np:hasProvenance dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_provenance;
    np:hasPublicationInfo dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_assertion a np:Assertion .
  
  dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_provenance a np:Provenance .
  
  dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_assertion {
  miriam-gene:5308 a ncit:C16612 .
  
  lld:C3495488 a ncit:C7057 .
  
  dgn-gda:DGN7210966014ea4baa083e16392651e665 sio:SIO_000628 miriam-gene:5308, lld:C3495488;
    a sio:SIO_001121 .
}

dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_provenance {
  dgn-np:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_assertion dcterms:description
      "[In addition to providing insight into the etiological mechanism of IH, IGDS and ARS, these results are consistent with the hypothesis that mutant PITX2 proteins that retain partial function result in milder anterior segment aberrations.]. 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:10958652;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP293120.RAESSGsyjMLCXUndD_zZPZUbLWJX8fEyVSE72mtWmrV2E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:58+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}