@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU> .
@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:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_head {
  this: np:hasAssertion dgn-np:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_assertion;
    np:hasProvenance dgn-np:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_provenance;
    np:hasPublicationInfo dgn-np:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_assertion a np:Assertion .
  
  dgn-np:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_provenance a np:Provenance .
  
  dgn-np:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_assertion {
  miriam-gene:4914 a ncit:C16612 .
  
  lld:C0010278 a ncit:C7057 .
  
  dgn-gda:DGN497d21edb09acb54d894d4a0f9b6896d sio:SIO_000628 miriam-gene:4914, lld:C0010278;
    a sio:SIO_001121 .
}

dgn-np:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_provenance {
  dgn-np:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_assertion dcterms:description
      "[However, more direct evidence for abnormal tyrosine kinase receptor signalling in AN has been provided by studies of craniosynostosis and skeletal dysplasia syndromes with AN, which have identified activating mutations in fibroblast growth factor receptors.]. 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:12452857;
    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:NP599735.RAtVJk1dX34FcYBskKSOC3LKHrB8szlp1CVhjELiuMNcU130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:38+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}