@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg
> .
@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:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_head
{
this:
np:hasAssertion
dgn-np:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_assertion
;
np:hasProvenance
dgn-np:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_provenance
;
np:hasPublicationInfo
dgn-np:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_assertion
a
np:Assertion
.
dgn-np:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_provenance
a
np:Provenance
.
dgn-np:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_assertion
{
miriam-gene:1579
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGNb50e81fcff7d6e5ff731ae79358c6abd
sio:SIO_000628
miriam-gene:1579
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_provenance
{
dgn-np:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_assertion
dcterms:description
"[This study tested the hypothesis that the CYP4A11 T8590C polymorphism is associated with higher BP or clinical outcomes in 732 black Americans with hypertensive renal disease participating in the African American Study of Kidney Disease (AASK).]. 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:18385420
;
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:NP804165.RAvqnjs9iArIbpFUiB0377sAWVRXm0H4Pl3a5rE_1oIGg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:13+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" .
}