@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo> .
@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/v4.0.0/void/> .
dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_head {
  this: np:hasAssertion dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_assertion ;
    np:hasProvenance dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_provenance ;
    np:hasPublicationInfo dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_assertion a np:Assertion .
  dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_provenance a np:Provenance .
  dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_assertion {
  miriam-gene:6657 a ncit:C16612 .
  lld:C0020635 a ncit:C7057 .
  dgn-gda:DGN45f2de7ba3ab53c3b71d6526c3a82376 sio:SIO_000628 miriam-gene:6657 , lld:C0020635 ;
    a sio:SIO_001121 .
}
dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_provenance {
  dgn-np:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_assertion dcterms:description "[Duplications and polyalanine expansions within the transcription factor SOX3 have recently been described in association with infundibular hypoplasia, hypopituitarism and variable mental retardation, whilst mutations in SOX2 are associated with variable hypopituitarism in association with learning difficulties, oesophageal atresia and anophthalmia.]. 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:18174732 ;
    prov:wasDerivedFrom dgn-void:befree-2016 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP648386.RAb-JzQ8O4VvM3HfHjbhOs-lywQAj51HByaI8ou_EaSPo130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:39+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 "v4.0.0.0" .
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}