@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM
> .
@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:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_head
{
this:
np:hasAssertion
dgn-np:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_assertion
;
np:hasProvenance
dgn-np:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_provenance
;
np:hasPublicationInfo
dgn-np:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_assertion
a
np:Assertion
.
dgn-np:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_provenance
a
np:Provenance
.
dgn-np:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_assertion
{
miriam-gene:6559
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN6291a72837ea4fd50a85ef3a00a802a3
sio:SIO_000628
miriam-gene:6559
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_provenance
{
dgn-np:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_assertion
dcterms:description
"[substitution of arginine for cysteine at position 919 increases Na transport function and supports the hypothesis that mutations in renal tubular Na transporters contribute to the development of primary hypertension by increasing renal Na reabsorption ]. 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:17885550
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP123322.RA9SwR_RtPko4JtT0-_Jg5KMldyT5QM-QekUQC-jyPXrM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:04+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" .
}