@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4
> .
@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 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:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_head
{
this:
np:hasAssertion
dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_assertion
;
np:hasProvenance
dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_provenance
;
np:hasPublicationInfo
dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_assertion
a
np:Assertion
.
dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_provenance
a
np:Provenance
.
dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_assertion
{
miriam-gene:185
a
ncit:C16612
.
lld:C0042580
a
ncit:C7057
.
dgn-gda:DGN7cb7b8d8f418aebf903e7bd5e987b0f3
sio:SIO_000628
miriam-gene:185
,
lld:C0042580
;
a
sio:SIO_001122
.
}
dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_provenance
{
dgn-np:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_assertion
dct:description
"[To detect the relation of the risk factors of primary VUR with the genetic polymorphism, the distribution of ACE, AT1 and AT2 genotypes after stratification by risk factors was also studied in the primary VUR patients.]. 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:14764974
;
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:NP48823.RAp3VRnQMJoZot1tt-SLz6xRrk8oCwKF5GxGkygYutvT4130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:22+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}