@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k> .
@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:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_head {
  this: np:hasAssertion dgn-np:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_assertion;
    np:hasProvenance dgn-np:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_provenance;
    np:hasPublicationInfo dgn-np:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_assertion a np:Assertion .
  
  dgn-np:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_provenance a np:Provenance .
  
  dgn-np:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_assertion {
  miriam-gene:79947 a ncit:C16612 .
  
  lld:C0559260 a ncit:C7057 .
  
  dgn-gda:DGNc9eb2ed130367029078a2cb7f1d81f46 sio:SIO_000628 miriam-gene:79947, lld:C0559260;
    a sio:SIO_001121 .
}

dgn-np:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_provenance {
  dgn-np:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_assertion dcterms:description
      "[The orthopaedic manifestations of congenital pseudarthrosis of the tibia (CPT) and scoliosis, along with other skeletal defects including sphenoid wing dysplasia, rib penciling, and gracile bones have been classically associated with NF1.]. 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:18248783;
    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:NP876623.RAsZXcEty67OjE4bMD3TuGiMLyXpnh23AbNRBFosvgM5k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:55+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" .
}