@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_head
{
this:
np:hasAssertion
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_assertion
;
np:hasProvenance
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_provenance
;
np:hasPublicationInfo
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_assertion
a
np:Assertion
.
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_provenance
a
np:Provenance
.
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_assertion
{
miriam-gene:2492
a
ncit:C16612
.
lld:C0085083
a
ncit:C7057
.
dgn-gda:DGNf43b634ca5351351dca2ccb85d21f317
sio:SIO_000628
miriam-gene:2492
,
lld:C0085083
;
a
sio:SIO_001121
.
}
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_provenance
{
dgn-np:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_assertion
dcterms:description
"[The paper focuses on the recent identification of mutations in the FSH receptor gene that display an increased sensitivity to hCG and are responsible for the development of spontaneous OHSS occurring during pregnancy.]. 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:16034183
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP505138.RAuDWTgjV2ND668K4LFN74ahEF9pj1kQMq7va0WNF0X2U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:34+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}