@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc
> .
@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:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_head
{
this:
np:hasAssertion
dgn-np:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_assertion
;
np:hasProvenance
dgn-np:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_provenance
;
np:hasPublicationInfo
dgn-np:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_assertion
a
np:Assertion
.
dgn-np:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_provenance
a
np:Provenance
.
dgn-np:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_assertion
{
miriam-gene:624
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN4421da2bbc0efad5686eee172c018730
sio:SIO_000628
miriam-gene:624
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_provenance
{
dgn-np:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_assertion
dcterms:description
"[The association of baseline fitness with risk of hypertension was nominally modified by genotype at markers within the angiotensin converting enzyme, angiotensinogen, BDKRB2 and NOS3 genes in blacks and the BDKRB2, endothelin-1 and PPARGC1A genes in whites.]. 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:20944660
;
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:NP558183.RADDFxik80lPojjREWvwMU0q4L6foESEu5ipwj9ZLb3Fc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}