@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0> .
@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:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_head {
  this: np:hasAssertion dgn-np:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_assertion;
    np:hasProvenance dgn-np:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_provenance;
    np:hasPublicationInfo dgn-np:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_assertion a np:Assertion .
  
  dgn-np:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_provenance a np:Provenance .
  
  dgn-np:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_assertion {
  miriam-gene:5294 a ncit:C16612 .
  
  lld:C0011644 a ncit:C7057 .
  
  dgn-gda:DGN36851359e74c6946e9cb82f8c4649ddd sio:SIO_000628 miriam-gene:5294, lld:C0011644;
    a sio:SIO_001121 .
}

dgn-np:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_provenance {
  dgn-np:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_assertion dcterms:description
      "[These results indicate that 1) the basal activity of PI3K is necessary for the COL1A2 mRNA stabilization in normal and scleroderma fibroblasts, 2) there is an unidentified FYVE domain protein specifically interacting with Smad3, and 3) the basal activity of PI3K and the FYVE domain protein are indispensable for the efficient TGF-beta/Smad3 signaling in normal fibroblasts and for the establishment of the constitutive activation of TGF-beta/Smad3 signaling in scleroderma fibroblasts.]. 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:15153536;
    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:NP817688.RAWkMbxT-EsOk9KN-XOKTtasJmqUR6s39SM-c8NKfVdc0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:21+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" .
}