@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k
> .
@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:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_head
{
this:
np:hasAssertion
dgn-np:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_assertion
;
np:hasProvenance
dgn-np:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_provenance
;
np:hasPublicationInfo
dgn-np:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_assertion
a
np:Assertion
.
dgn-np:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_provenance
a
np:Provenance
.
dgn-np:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_assertion
{
miriam-gene:885
a
ncit:C16612
.
lld:C0023269
a
ncit:C7057
.
dgn-gda:DGNa6287ae7ccf89cc616664dd3ba35c15d
sio:SIO_000628
miriam-gene:885
,
lld:C0023269
;
a
sio:SIO_001121
.
}
dgn-np:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_provenance
{
dgn-np:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_assertion
dcterms:description
"[Since discrepancies between mRNA levels and CCK2R binding sites were noticed, we searched for abnormally spliced variants in tumors from various origins having been previously reported to frequently express cholecystokinin receptors, such as medullary thyroid carcinomas, gastrointestinal stromal tumors, leiomyomas and leiomyosarcomas, and gastroenteropancreatic tumors.]. 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:22040601
;
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:NP665873.RAQ5LcCNlQJ2ZHboafr7S6aTPKx07yGoQhXiCnnxr__-k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}