@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_assertion
;
np:hasProvenance
dgn-np:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_provenance
;
np:hasPublicationInfo
dgn-np:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_assertion
a
np:Assertion
.
dgn-np:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_provenance
a
np:Provenance
.
dgn-np:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNc82be3a1dd33c0985b777036d40b563b
sio:SIO_000628
miriam-gene:1813
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_provenance
{
dgn-np:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_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:NP205415.RAoTKQWWqKJ1XY7rWzIXA7zur6L4mt-0pj5Cnp_hLW4Hs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:53+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" .
}