@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU
> .
@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:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_head
{
this:
np:hasAssertion
dgn-np:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_assertion
;
np:hasProvenance
dgn-np:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_provenance
;
np:hasPublicationInfo
dgn-np:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_assertion
a
np:Assertion
.
dgn-np:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_provenance
a
np:Provenance
.
dgn-np:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_assertion
{
miriam-gene:7200
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGNe66817f4524ee965dd4fe58f54faec3e
sio:SIO_000628
miriam-gene:7200
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_provenance
{
dgn-np:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_assertion
dcterms:description
"[Endocrinological identification of silent somatotroph adenomas in combination with paradoxical responses of GH in TRH or GnRH provocation tests may elucidate the increasing number of silent somatotroph adenomas that have been regarded as mammotroph or clinically inactive 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:11209812
;
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:NP800702.RATRErP191iJKW3Cu91LGCN9H1xIw3I1EoMMD2bUK3zWU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}