@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA
> .
@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:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_head
{
this:
np:hasAssertion
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_assertion
;
np:hasProvenance
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_provenance
;
np:hasPublicationInfo
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_assertion
a
np:Assertion
.
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_provenance
a
np:Provenance
.
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_assertion
{
miriam-gene:3162
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGN51f264362cb4422d70dc9d421872c8ff
sio:SIO_000628
miriam-gene:3162
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_provenance
{
dgn-np:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_assertion
dcterms:description
"[We hypothesized that this gene might be responsible for the variation of susceptibility to essential hypertension (EH) and BP and investigated three polymorphisms in HMOX1 (i.e., the (GT)n repeat in the HMOX1 promoter and single-nucleotide polymorphisms (SNPs) rs2071746 and rs2071749) in population-based samples of 789 Han Chinese from Xinjiang, China.]. 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:21275653
;
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:NP510154.RAiBP3hmNqJiKsCt0_d_gNAQ2LsGyEeNkUWsPhI-OjOfA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}