@prefix bfo: .
@prefix this: .
@prefix rdfs: .
@prefix xsd: .
@prefix sio: .
@prefix ncit: .
@prefix lld: .
@prefix miriam-gene: .
@prefix miriam-pubmed: .
@prefix wi: .
@prefix prov: .
@prefix pav: .
@prefix prv: .
@prefix dcterms: .
@prefix np: .
@prefix dgn-np: .
@prefix dgn-gda: .
@prefix dgn-void: .
dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_head {
this: np:hasAssertion dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_assertion;
np:hasProvenance dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_provenance;
np:hasPublicationInfo dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_publicationInfo;
a np:Nanopublication .
dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_assertion a np:Assertion .
dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_provenance a np:Provenance .
dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_publicationInfo a
np:PublicationInfo .
}
dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_assertion {
miriam-gene:9049 a ncit:C16612 .
lld:C0033375 a ncit:C7057 .
dgn-gda:DGN404d839f5219de23029f446ecf411458 sio:SIO_000628 miriam-gene:9049, lld:C0033375;
a sio:SIO_001121 .
}
dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_provenance {
dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_assertion dcterms:description
"[AIP variants were detected in 3% of the 127 patients, comprising four of 48 patients with acromegaly (8%), 0 of 43 with prolactinomas, 0 of the 20 patients with non-functioning adenomas, 0 of 15 with corticotroph adenomas and 0 of one with a thyrotroph adenomas.]. 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:25184284;
prov:wasDerivedFrom dgn-void:befree-20150227;
prov:wasGeneratedBy bfo:ECO_0000203 .
dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^xsd:date .
dgn-void:source_evidence_literature a bfo:ECO_0000212;
rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP814154.RAhEUlqQLQeeLmiHCBh-w3QQzWWLo8dutIjGoYFECbWeI130_publicationInfo {
this: dcterms:created "2015-08-25T14:45:53+02:00"^^xsd:dateTime;
dcterms:rights ;
dcterms:rightsHolder dgn-void:IBIGroup;
dcterms:subject sio:SIO_000983;
prv:usedData dgn-void:disgenetv3.0rdf;
pav:authoredBy , ,
, , ;
pav:createdBy ;
pav:version "v3.0.0.0" .
dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}