@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA> .
@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:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_head {
  this: np:hasAssertion dgn-np:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_assertion;
    np:hasProvenance dgn-np:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_provenance;
    np:hasPublicationInfo dgn-np:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_assertion a np:Assertion .
  
  dgn-np:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_provenance a np:Provenance .
  
  dgn-np:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_assertion {
  miriam-gene:415 a ncit:C16612 .
  
  lld:C0008445 a ncit:C7057 .
  
  dgn-gda:DGNe9e17218b18e68ed0473c92fbc711e4d sio:SIO_000628 miriam-gene:415, lld:C0008445;
    a sio:SIO_001121 .
}

dgn-np:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_provenance {
  dgn-np:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_assertion dcterms:description
      "[First, the absence of stippled epiphyses on radiograms should not be considered an exclusion criteria for ARSE mutation screening in patients with other features of the disease, especially after the neonatal period.]. 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:19839041;
    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:NP770052.RAp9dhWifeOLh3FcY0Y2RP02V6IhU96l7agAcXSKYAXYA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:34+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: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" .
}