@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0> .
@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:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_head {
   this: np:hasAssertion dgn-np:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_assertion ;
    np:hasProvenance dgn-np:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_provenance ;
    np:hasPublicationInfo dgn-np:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_assertion a np:Assertion .
  dgn-np:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_provenance a np:Provenance .
  dgn-np:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_assertion {
   miriam-gene:7483 a ncit:C16612 .
  lld:C1306459 a ncit:C7057 .
  dgn-gda:DGN334d52216120d242ae4dff6968ede79f sio:SIO_000628 miriam-gene:7483 , lld:C1306459 ;
    a sio:SIO_001121 .
}
dgn-np:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_provenance {
   dgn-np:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_assertion dcterms:description "[Because these WNT gene clusters might be fragile sites in the human genome, implication of WNT3 or WNT3A in cancer as well as implication of WNT14 or WNT14B in connective tissue disease and congenital joint malformation should be elucidated in the future.]. 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:12011973 ;
    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:NP777819.RA1aedrM0saxAUjrteUXzBDejfiINShXx6gReFsWgjrD0130_publicationInfo {
   this: dcterms:created "2015-08-25T14:45:30+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" .
}