@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA
> .
@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:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_head
{
this:
np:hasAssertion
dgn-np:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_assertion
;
np:hasProvenance
dgn-np:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_provenance
;
np:hasPublicationInfo
dgn-np:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_assertion
a
np:Assertion
.
dgn-np:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_provenance
a
np:Provenance
.
dgn-np:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_assertion
{
miriam-gene:2492
a
ncit:C16612
.
lld:C0014175
a
ncit:C7057
.
dgn-gda:DGNf0021b33263b1c91580986457e6a4b39
sio:SIO_000628
miriam-gene:2492
,
lld:C0014175
;
a
sio:SIO_001121
.
}
dgn-np:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_provenance
{
dgn-np:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_assertion
dcterms:description
"[Six hundred thirty-seven Taiwanese Chinese women including 300 patients with endometriosis and 337 controls without endometriosis were enrolled to investigate the association between nonsynonymous single nucleotide polymorphism of the FSH receptor gene and the risk of endometriosis.]. 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:20817169
;
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:NP390887.RAzH_yoU4h73AfgDHfITNs8pc3kEToCH_HzYzDUmuHsuA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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" .
}