@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do
> .
@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:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_head
{
this:
np:hasAssertion
dgn-np:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_assertion
;
np:hasProvenance
dgn-np:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_provenance
;
np:hasPublicationInfo
dgn-np:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_assertion
a
np:Assertion
.
dgn-np:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_provenance
a
np:Provenance
.
dgn-np:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_assertion
{
miriam-gene:7067
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNf01d3349fc0c2dc2fb86d215c04ed641
sio:SIO_000628
miriam-gene:7067
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_provenance
{
dgn-np:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_assertion
dcterms:description
"[For the first time, our study showed associations between the THRA rs939348 polymorphism and systolic BP and the risk of hypertension but not with CHD, although we admit that the statistical power available to study any relationship with CHD was very limited.]. 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:21654857
;
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:NP508581.RAHJC0vyjZOXPkyJ8WcB9Hh8CJP7Z-8ZEHiWGJys8R6do130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}