@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM
> .
@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:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_head
{
this:
np:hasAssertion
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_assertion
;
np:hasProvenance
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_provenance
;
np:hasPublicationInfo
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_assertion
a
np:Assertion
.
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_provenance
a
np:Provenance
.
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_assertion
{
miriam-gene:2778
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN815c7df1c7aa396ffe1bc4f374a25416
sio:SIO_000628
miriam-gene:2778
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_provenance
{
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_assertion
dcterms:description
"[To understand genetic determinants of androgen excess, insulin resistance, and obesity in polycystic ovary syndrome (PCOS), we investigated the effect of the common GNAS1 T393C polymorphism on the phenotype of German PCOS women.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:17062894
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP17022.RAmuirrb5zBzpeULK7o55l4HS182cgTjr-fX4Hht-haaM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:06+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" .
}