@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA
> .
@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:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_head
{
this:
np:hasAssertion
dgn-np:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_assertion
;
np:hasProvenance
dgn-np:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_provenance
;
np:hasPublicationInfo
dgn-np:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_assertion
a
np:Assertion
.
dgn-np:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_provenance
a
np:Provenance
.
dgn-np:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0017661
a
ncit:C7057
.
dgn-gda:DGNf7189180233b412df05c646d96e4bed4
sio:SIO_000628
miriam-gene:183
,
lld:C0017661
;
a
sio:SIO_001122
.
}
dgn-np:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_provenance
{
dgn-np:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_assertion
dcterms:description
"[Although AGT M235T was not associated with the development of hypertension in either sex, men with M235T TT were found to be at an increased risk of IgAN progression compared to those with the other genotypes (p = 0.019).]. 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:19729965
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP75547.RAoUGPRN0V06o4pNjKIwHawT_QjTIJVGMOs1whihdv9qA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:37+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" .
}