@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg
> .
@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:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_head
{
this:
np:hasAssertion
dgn-np:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_assertion
;
np:hasProvenance
dgn-np:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance
;
np:hasPublicationInfo
dgn-np:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_assertion
a
np:Assertion
.
dgn-np:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance
a
np:Provenance
.
dgn-np:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0042580
a
ncit:C7057
.
dgn-gda:DGN7c7acb901f1e67855213e16b01e3e6d8
sio:SIO_000628
miriam-gene:1636
,
lld:C0042580
;
a
sio:SIO_001121
.
}
dgn-np:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_provenance
{
dgn-np:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_assertion
dcterms:description
"[This study demonstrates that ACE genotype frequencies are similar in index patients with VUR and their unaffected siblings, thus suggesting that the ACE gene is not involved in the development of familial VUR.]. 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:11409168
;
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:NP491199.RAEpbHrQ8jT4Hb_O0nFM7M0OUz6N7eZd2lZQ_VwTq-dWg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}