@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0> .
@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:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_head {
  this: np:hasAssertion dgn-np:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_assertion;
    np:hasProvenance dgn-np:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_provenance;
    np:hasPublicationInfo dgn-np:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_assertion a np:Assertion .
  
  dgn-np:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_provenance a np:Provenance .
  
  dgn-np:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_assertion {
  miriam-gene:6095 a ncit:C16612 .
  
  lld:C0265205 a ncit:C7057 .
  
  dgn-gda:DGN96340b54d096feed94fe24eb1a246e30 sio:SIO_000628 miriam-gene:6095, lld:C0265205;
    a sio:SIO_001121 .
}

dgn-np:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_provenance {
  dgn-np:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_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:NP662572.RAZ-9wZNnwKlKgRv_lSMlSqCJdb3bpSLJplcGOp_q_lA0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:40+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" .
}