@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY
> .
@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:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_head
{
this:
np:hasAssertion
dgn-np:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_assertion
;
np:hasProvenance
dgn-np:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_provenance
;
np:hasPublicationInfo
dgn-np:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_assertion
a
np:Assertion
.
dgn-np:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_provenance
a
np:Provenance
.
dgn-np:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C0409957
a
ncit:C7057
.
dgn-gda:DGN4070f52d921ae5fb92b9a4ae67d06ab5
sio:SIO_000628
miriam-gene:2099
,
lld:C0409957
;
a
sio:SIO_001122
.
}
dgn-np:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_provenance
{
dgn-np:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_assertion
dcterms:description
"[There was also a suggestive interaction between the HFE rs179945 and the ESR1 rs9340799, and the carriage of the minor allele of either of these SNPs was associated with an increased risk of symptomatic DIP OA (2.1, 1.3-2.5).]. 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:24825461
;
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:NP1182246.RAgeJklRHEqXtTVsqrpR085ls8nZukpFN5WkboqMaIqzY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:41+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" .
}