@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs
> .
@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:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_head
{
this:
np:hasAssertion
dgn-np:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_assertion
;
np:hasProvenance
dgn-np:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_provenance
;
np:hasPublicationInfo
dgn-np:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_assertion
a
np:Assertion
.
dgn-np:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_provenance
a
np:Provenance
.
dgn-np:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_assertion
{
miriam-gene:1392
a
ncit:C16612
.
lld:C0221406
a
ncit:C7057
.
dgn-gda:DGN2a75aa77261306320ef0909990cbc8dd
sio:SIO_000628
miriam-gene:1392
,
lld:C0221406
;
a
sio:SIO_001121
.
}
dgn-np:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_provenance
{
dgn-np:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_assertion
dcterms:description
"[Based on existing data, the desmopressin test is regarded as an alternative to the CRH stimulation test and, when given in combination with CRH, it has been suggested to completely discriminate between patients with CD and EAS.]. 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:11932296
;
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:NP234503.RAEW81IYh9EYKMlPtA_I1WmdJk1ghDp1IfarGB_hPAkMs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:11+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" .
}