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http://rdf.disgenet.org/nanopublications.trig#NP845884.RAM4BDUF34O2aHfZ4rj8cVPnR4NWdcMEFdu6gbZN5HIf8
> .
@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:NP845884.RAM4BDUF34O2aHfZ4rj8cVPnR4NWdcMEFdu6gbZN5HIf8130_head
{
this:
np:hasAssertion
dgn-np:NP845884.RAM4BDUF34O2aHfZ4rj8cVPnR4NWdcMEFdu6gbZN5HIf8130_assertion
;
np:hasProvenance
dgn-np:NP845884.RAM4BDUF34O2aHfZ4rj8cVPnR4NWdcMEFdu6gbZN5HIf8130_provenance
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np:hasPublicationInfo
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a
np:Nanopublication
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dgn-np:NP845884.RAM4BDUF34O2aHfZ4rj8cVPnR4NWdcMEFdu6gbZN5HIf8130_assertion
a
np:Assertion
.
dgn-np:NP845884.RAM4BDUF34O2aHfZ4rj8cVPnR4NWdcMEFdu6gbZN5HIf8130_provenance
a
np:Provenance
.
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a
np:PublicationInfo
.
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{
miriam-gene:10205
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN5646c36bcdb22fadee96d47d47acefe6
sio:SIO_000628
miriam-gene:10205
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP845884.RAM4BDUF34O2aHfZ4rj8cVPnR4NWdcMEFdu6gbZN5HIf8130_provenance
{
dgn-np:NP845884.RAM4BDUF34O2aHfZ4rj8cVPnR4NWdcMEFdu6gbZN5HIf8130_assertion
dcterms:description
"[Among 11 OTC polymorphisms that were originally selected from databases, the tag single-nucleotide polymorphism (SNP) rs5963409 and the independent SNP rs1800321 were tested for association with hypertension in two independent population samples recruited in Northern (Multinational MONItoring of trends and determinants in CArdiovascular disease (MONICA) study, n = 1,138) and Western (Etude du Vieillissement Artériel (EVA) study, n = 1,166) France.]. 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:19574962
;
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:NP845884.RAM4BDUF34O2aHfZ4rj8cVPnR4NWdcMEFdu6gbZN5HIf8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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
<
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> , <
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
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dgn-void:disgenetrdf
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}