@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw
> .
@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:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_head
{
this:
np:hasAssertion
dgn-np:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_assertion
a
np:Assertion
.
dgn-np:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_provenance
a
np:Provenance
.
dgn-np:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_assertion
{
miriam-gene:9049
a
ncit:C16612
.
lld:C0032019
a
ncit:C7057
.
dgn-gda:DGN50909dd0b381f6a4aba75c30dd5ce95f
sio:SIO_000628
miriam-gene:9049
,
lld:C0032019
;
a
sio:SIO_001121
.
}
dgn-np:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_provenance
{
dgn-np:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_assertion
dcterms:description
"[The objectives of this study were to examine the frequency of the three AIP germline mutations in U.S. patients harboring sporadic pituitary tumors and to correlate clinical features of pituitary tumors with these mutations, if they exist in these 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:17018653
;
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:NP173242.RA2ygIAtT5t6FKHRGpw6GV72arQwqavxHGIoOA9My9FTw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}