@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP73236.RA4dGu1gTgRpn-FG9oWi4zhYyXJReLQdalNEPvc07-UZM
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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:NP73236.RA4dGu1gTgRpn-FG9oWi4zhYyXJReLQdalNEPvc07-UZM130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP73236.RA4dGu1gTgRpn-FG9oWi4zhYyXJReLQdalNEPvc07-UZM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP73236.RA4dGu1gTgRpn-FG9oWi4zhYyXJReLQdalNEPvc07-UZM130_assertion
a
np:Assertion
.
dgn-np:NP73236.RA4dGu1gTgRpn-FG9oWi4zhYyXJReLQdalNEPvc07-UZM130_provenance
a
np:Provenance
.
dgn-np:NP73236.RA4dGu1gTgRpn-FG9oWi4zhYyXJReLQdalNEPvc07-UZM130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:3305
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNc1c6de914c89f4d59f526299c4945cc1
sio:SIO_000628
miriam-gene:3305
,
lld:C0020538
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.
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dgn-np:NP73236.RA4dGu1gTgRpn-FG9oWi4zhYyXJReLQdalNEPvc07-UZM130_provenance
{
dgn-np:NP73236.RA4dGu1gTgRpn-FG9oWi4zhYyXJReLQdalNEPvc07-UZM130_assertion
dcterms:description
"[In this study, we focused on five polymorphisms in three genes (HSPA1A, HSPA1B, and HSPA1L) of Hsp70 family to explore the genetic contribution, alone and in combination, of these polymorphisms to essential hypertension risk in a Uygur population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:19085089
;
prov:wasDerivedFrom
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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 .
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dgn-np:NP73236.RA4dGu1gTgRpn-FG9oWi4zhYyXJReLQdalNEPvc07-UZM130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
dgn-void:disgenetrdf
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> , <
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> , <
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> ;
pav:createdBy
<
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