@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY> .
@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:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_head {
  this: np:hasAssertion dgn-np:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_assertion ;
    np:hasProvenance dgn-np:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_provenance ;
    np:hasPublicationInfo dgn-np:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_assertion a np:Assertion .
  dgn-np:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_provenance a np:Provenance .
  dgn-np:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_assertion {
  miriam-gene:2969 a ncit:C16612 .
  lld:C0679466 a ncit:C7057 .
  dgn-gda:DGN183ca17d506f181b654f94fb58496576 sio:SIO_000628 miriam-gene:2969 , lld:C0679466 ;
    a sio:SIO_001121 .
}
dgn-np:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_provenance {
  dgn-np:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_assertion dcterms:description "[Our results are consistent with the hypothesis that hemizygosity of the GTF2IRD1 and GTF2I genes might be involved in the facial dysmorphisms and in the specific motor and cognitive deficits observed in WBS patients.]. 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:19568270 ;
    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:NP643769.RATSSsac-qXnahS54KyhgoTOAyYwb3asnjcQiQS_dqxKY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:28+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" .
}