@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4
> .
@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:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_head
{
this:
np:hasAssertion
dgn-np:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_assertion
;
np:hasProvenance
dgn-np:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_provenance
;
np:hasPublicationInfo
dgn-np:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_assertion
a
np:Assertion
.
dgn-np:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_provenance
a
np:Provenance
.
dgn-np:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_assertion
{
miriam-gene:2492
a
ncit:C16612
.
lld:C0085083
a
ncit:C7057
.
dgn-gda:DGNe9f6d3d98f1f78ed5b738150883cebdf
sio:SIO_000628
miriam-gene:2492
,
lld:C0085083
;
a
sio:SIO_001121
.
}
dgn-np:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_provenance
{
dgn-np:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_assertion
dcterms:description
"[The recent identification of mutations in the FSH receptor gene, which display an increased sensitivity to hCG and are responsible for the development of spontaneous ovarian hyperstimulation syndrome (OHSS), provides for the first time the molecular basis for the physiopathology of spontaneous OHSS.]. 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:14998941
;
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:NP434027.RALqSqXcd-8Ppx8i279gETFzJKVMcwpg-CBQlI-7CH0f4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:02+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" .
}