@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_head
{
this:
np:hasAssertion
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_assertion
;
np:hasProvenance
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_provenance
;
np:hasPublicationInfo
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_assertion
a
np:Assertion
.
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_provenance
a
np:Provenance
.
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN1798dcec8fc82e43ff2ddbad61c59d7e
sio:SIO_000628
miriam-gene:5972
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_provenance
{
dgn-np:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_assertion
dcterms:description
"[Additional cohorts of patients with primary aldosteronism and metabolic syndrome, particularly African Americans, should be screened for ARMC5 sequence variants because these may underlie part of the known increased predisposition of African Americans to low renin hypertension.]. 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:25822102
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1274759.RAw_35FEgXyXKl8r8R8I9o27Qdyv2djB9I4sv0BMdoZlU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:24+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}