@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U
> .
@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:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_head
{
this:
np:hasAssertion
dgn-np:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_assertion
;
np:hasProvenance
dgn-np:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_provenance
;
np:hasPublicationInfo
dgn-np:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_assertion
a
np:Assertion
.
dgn-np:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_provenance
a
np:Provenance
.
dgn-np:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGNb6bc3bca79cdf5cd8589c345f7bbfe9e
sio:SIO_000628
miriam-gene:1636
,
lld:C0022661
;
a
sio:SIO_001122
.
}
dgn-np:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_provenance
{
dgn-np:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_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.]. 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:NP49460.RAV0SRSRlYRHbazBfyNRYsbjKjbcCqkAO2_YA3SYFTu5U130_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" .
}