@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8
> .
@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 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:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_head
{
this:
np:hasAssertion
dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_assertion
;
np:hasProvenance
dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_provenance
;
np:hasPublicationInfo
dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_assertion
a
np:Assertion
.
dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_provenance
a
np:Provenance
.
dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_assertion
{
miriam-gene:729230
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN4e702c8e57a9107d15927fce5b52e9d5
sio:SIO_000628
miriam-gene:729230
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_provenance
{
dgn-np:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_assertion
dct:description
"[ These results suggest that two and one genes may be susceptibility loci for hypertension in Japanese men and women, respectively, and that genotyping of these polymorphisms may prove informative for prediction of the genetic risk for hypertension.]. 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:15046042
;
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:NP59810.RA2Mc7AqPCyU7ZkjjbqxQS709Vk_PPqMcqIJ3aRxzV-J8130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}