@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY> .
@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:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_head {
  this: np:hasAssertion dgn-np:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_assertion;
    np:hasProvenance dgn-np:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_provenance;
    np:hasPublicationInfo dgn-np:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_assertion a np:Assertion .
  
  dgn-np:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_provenance a np:Provenance .
  
  dgn-np:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_assertion {
  miriam-gene:4920 a ncit:C16612 .
  
  lld:C0221357 a ncit:C7057 .
  
  dgn-gda:DGNb2ba955040e14014fc3f722e8d9a7dae sio:SIO_000628 miriam-gene:4920, lld:C0221357;
    a sio:SIO_001121 .
}

dgn-np:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_provenance {
  dgn-np:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_assertion dcterms:description
      "[The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. 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:12011143;
    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:NP212004.RAS_okxRI24-V7iGzAhU1CMbzBIx375wsKZecJVG_piNY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:57+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" .
}