@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo> .
@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:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_head {
  this: np:hasAssertion dgn-np:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_assertion ;
    np:hasProvenance dgn-np:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_provenance ;
    np:hasPublicationInfo dgn-np:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_assertion a np:Assertion .
  dgn-np:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_provenance a np:Provenance .
  dgn-np:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_assertion {
  miriam-gene:9232 a ncit:C16612 .
  lld:C0032000 a ncit:C7057 .
  dgn-gda:DGN1f539657c42ee7b6a8920a75e87e04a5 sio:SIO_000628 miriam-gene:9232 , lld:C0032000 ;
    a sio:SIO_001121 .
}
dgn-np:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_provenance {
  dgn-np:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_assertion dcterms:description "[Though no significant association was found between PTTG1 haplotypes and the risk of pituitary adenoma, this is the first report on the association of individual PTTG1 SNPs or PTTG1 haplotypes with the risk of pituitary adenoma based on a solid study; it will provide an important reference for future studies on the association between genetic alterations in PTTG1 and the risk of pituitary adenoma or other tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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:NP316828.RA_fvM3KaAbPp7tmreRMBkUuHi1qCMBlZ0msp_gguj1qo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:04+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> ;
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    pav:version "v2.1.0.0" .
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}