@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc
> .
@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:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_head
{
this:
np:hasAssertion
dgn-np:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_assertion
;
np:hasProvenance
dgn-np:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_provenance
;
np:hasPublicationInfo
dgn-np:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_assertion
a
np:Assertion
.
dgn-np:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_provenance
a
np:Provenance
.
dgn-np:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_assertion
{
miriam-gene:1113
a
ncit:C16612
.
lld:C0848548
a
ncit:C7057
.
dgn-gda:DGN2d292c32faba6b12a91344f093a0fa70
sio:SIO_000628
miriam-gene:1113
,
lld:C0848548
;
a
sio:SIO_001121
.
}
dgn-np:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_provenance
{
dgn-np:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_assertion
dcterms:description
"[Changes in storage and release of CHGA in clinical and experimental hypertension prompted us to study whether genetic variation at the CHGA locus might contribute to alterations in autonomic function, and hence hypertension and its target organ consequences such as hypertensive renal disease (nephrosclerosis).]. 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:21061160
;
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:NP600270.RASyvjyp54vfP5f-qt35xxFBZ-S6k4wSUmpzrepmk3KKc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}