@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q> .
@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:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_head {
  this: np:hasAssertion dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_assertion ;
    np:hasProvenance dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_assertion a np:Assertion .
  dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_provenance a np:Provenance .
  dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_assertion {
  miriam-gene:2263 a ncit:C16612 .
  lld:C0265269 a ncit:C7057 .
  dgn-gda:DGN2e923a97bccb889daac7f9abbb774226 sio:SIO_000628 miriam-gene:2263 , lld:C0265269 ;
    a sio:SIO_001121 .
}
dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_provenance {
  dgn-np:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_assertion dcterms:description "[Moreover, the nearly identical conformation of WT FGFR2 kinase and the A628T LADD mutant to either the phosphorylated FGFR2 or FGFR2 harboring pathological activating mutations in the kinase hinge region suggests that FGFR autoinhibition and activation are better explained by changes in the conformational dynamics of the kinase rather than by static crystallographic snapshots of minor structural variations.]. 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:18056630 ;
    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:NP432655.RAE8efOLKjK1W_h2Ci6XUwfUsXz4o6APAiC1GZOyjz15Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:16+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" .
}