@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y
> .
@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:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_head
{
this:
np:hasAssertion
dgn-np:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_assertion
;
np:hasProvenance
dgn-np:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_assertion
a
np:Assertion
.
dgn-np:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_provenance
a
np:Provenance
.
dgn-np:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_assertion
{
miriam-gene:118
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGNc3859c15b7667cfcd269a6df8df2c209
sio:SIO_000628
miriam-gene:118
,
lld:C0022661
;
a
sio:SIO_001122
.
}
dgn-np:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_provenance
{
dgn-np:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_assertion
dcterms:description
"[ The ADD genotype is predictive of the course of renal function loss in an unselected renal population and influences the effect of the ACE genotype to modulate the rate of progression to ESRD. Thus, the ADD genotype may play a role for the understanding of interindividual differences in the course of renal diseases.]. 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:11918733
;
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:NP49291.RAtX2g_h-lESti-2RaI4EaVFQZW6ZFZ3zRSO1uX3x7e0Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}