@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk
> .
@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:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_head
{
this:
np:hasAssertion
dgn-np:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_assertion
;
np:hasProvenance
dgn-np:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_provenance
;
np:hasPublicationInfo
dgn-np:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_assertion
a
np:Assertion
.
dgn-np:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_provenance
a
np:Provenance
.
dgn-np:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_assertion
{
miriam-gene:840
a
ncit:C16612
.
lld:C0279628
a
ncit:C7057
.
dgn-gda:DGNa18e317227c33ac5f6da2f89bd77a9b9
sio:SIO_000628
miriam-gene:840
,
lld:C0279628
;
a
sio:SIO_001122
.
}
dgn-np:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_provenance
{
dgn-np:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_assertion
dcterms:description
"[In conclusion, this study suggests that the genetic variants of CASP7 and CASP9 in the apoptosis pathway may be important predictive markers for EA susceptibility and that PGR in the sex hormone signaling pathway may be associated with the gender differences in EA risk.]. 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:20453000
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP90988.RAQ3uYT4Z2PcQ1z-sRn2950vd8q6CdMBOPKd9KsRr_Kyk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:45+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" .
}