@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo
> .
@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:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_head
{
this:
np:hasAssertion
dgn-np:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_assertion
;
np:hasProvenance
dgn-np:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_provenance
;
np:hasPublicationInfo
dgn-np:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_assertion
a
np:Assertion
.
dgn-np:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_provenance
a
np:Provenance
.
dgn-np:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_assertion
{
miriam-gene:2099
a
ncit:C16612
.
lld:C1455780
a
ncit:C7057
.
dgn-gda:DGNf16923ecdaf0b3179d075bee588dc7b2
sio:SIO_000628
miriam-gene:2099
,
lld:C1455780
;
a
sio:SIO_001122
.
}
dgn-np:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_provenance
{
dgn-np:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_assertion
dcterms:description
"[ We have demonstrated that the PvuII polymorphism in the ORalpha gene is related to both the presence of AS in postmenopausal women and to lipid levels in adolescent females, suggesting that this polymorphism may influence the risk of AS partly by affecting lipid levels.]. 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:12859695
;
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:NP44789.RACwL6aAoO5qlYyY4UpUe9WBfubS91E_1PKWaKQq4gWOo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}