@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M> .
@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/v3.0.0/void/> .

dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_head {
  this: np:hasAssertion dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_assertion;
    np:hasProvenance dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_provenance;
    np:hasPublicationInfo dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_assertion a np:Assertion .
  
  dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_provenance a np:Provenance .
  
  dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0029434 a ncit:C7057 .
  
  dgn-gda:DGN551607efdc0b89f3b04382cf8ab19191 sio:SIO_000628 miriam-gene:7248, lld:C0029434;
    a sio:SIO_001121 .
}

dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_provenance {
  dgn-np:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_assertion dcterms:description
      "[Eleven paternal diseases were discovered, which were Noonan-like syndrome (1), paternal cervical anomalies (1), Goldenhar syndrome (1), dominant autosomal arthrogryposis (1), osteogenesis imperfecta (3), tuberous sclerosis (1), dominant transposition of great vessels (1), Weyers acrofacial dysostosis (1), and autosomal dominant holoprosencephaly (1).]. 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:17139695;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP759113.RAno84_bibuRr__9r149q4p_oiyJtn1vPb6662xYzeU5M130_publicationInfo {
  this: dcterms:created "2015-08-25T14:45:18+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>,
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}