@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U
> .
@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:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_head
{
this:
np:hasAssertion
dgn-np:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_assertion
;
np:hasProvenance
dgn-np:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_provenance
;
np:hasPublicationInfo
dgn-np:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_assertion
a
np:Assertion
.
dgn-np:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_provenance
a
np:Provenance
.
dgn-np:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0029408
a
ncit:C7057
.
dgn-gda:DGN012d2c0d110325f711aa8e41396af423
sio:SIO_000628
miriam-gene:1588
,
lld:C0029408
;
a
sio:SIO_001121
.
}
dgn-np:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_provenance
{
dgn-np:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_assertion
dcterms:description
"[The aim of this study was to explore the association of two common polymorphisms within the aromatase (CYP19A1) and estrogen receptor (ER) alpha (ESR1) genes with severe OA of the lower limbs.]. 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:20417295
;
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:NP265341.RAkB-ojQG8DjmcjnenN86xTykj248a88F-kPKmvsB_Z_U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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" .
}