@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP925180.RAwyOXmWg_WzieU6t1rBMa1TeYZivJFtsYoSTamXOpCHg
> .
@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#
> .
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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
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP925180.RAwyOXmWg_WzieU6t1rBMa1TeYZivJFtsYoSTamXOpCHg130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP925180.RAwyOXmWg_WzieU6t1rBMa1TeYZivJFtsYoSTamXOpCHg130_assertion
a
np:Assertion
.
dgn-np:NP925180.RAwyOXmWg_WzieU6t1rBMa1TeYZivJFtsYoSTamXOpCHg130_provenance
a
np:Provenance
.
dgn-np:NP925180.RAwyOXmWg_WzieU6t1rBMa1TeYZivJFtsYoSTamXOpCHg130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:8129
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN8ffe8bf52b98af39ceab751ab7ee360f
sio:SIO_000628
miriam-gene:8129
,
lld:C0020538
;
a
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.
}
dgn-np:NP925180.RAwyOXmWg_WzieU6t1rBMa1TeYZivJFtsYoSTamXOpCHg130_provenance
{
dgn-np:NP925180.RAwyOXmWg_WzieU6t1rBMa1TeYZivJFtsYoSTamXOpCHg130_assertion
dcterms:description
"[Due to the controversial results about the role of the ATR1 gene locus in hypertension and understanding that ethnic origin should be carefully considered in studying the association between gene polymorphism and disease etiology, we investigated the role of A1166C polymorphism in Serbian hypertensives.]. 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:12482634
;
prov:wasDerivedFrom
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prov:wasGeneratedBy
eco:ECO_0000203
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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 .
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dgn-np:NP925180.RAwyOXmWg_WzieU6t1rBMa1TeYZivJFtsYoSTamXOpCHg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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