@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM
> .
@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:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_head
{
this:
np:hasAssertion
dgn-np:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_assertion
;
np:hasProvenance
dgn-np:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_provenance
;
np:hasPublicationInfo
dgn-np:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_assertion
a
np:Assertion
.
dgn-np:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_provenance
a
np:Provenance
.
dgn-np:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNefc99cac719372483f720aebd6945c62
sio:SIO_000628
miriam-gene:1813
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_provenance
{
dgn-np:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_assertion
dcterms:description
"[We have previously reported an association of the A2 allele of the dopamine D2 receptor (DRD2) TaqI polymorphism with increased blood pressure in normoglycaemic Chinese subjects, but conversely possibly with decreased indices of obesity.]. 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:11894971
;
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:NP791352.RAqOUaeWQUCXO0tuDHStq_Rm4eVVAa4R2WflSitebcLiM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:05+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" .
}