@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU
> .
@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:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_head
{
this:
np:hasAssertion
dgn-np:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_assertion
;
np:hasProvenance
dgn-np:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_provenance
;
np:hasPublicationInfo
dgn-np:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_assertion
a
np:Assertion
.
dgn-np:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_provenance
a
np:Provenance
.
dgn-np:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0017665
a
ncit:C7057
.
dgn-gda:DGNa3489638352758252aa3a04fd3f6b7be
sio:SIO_000628
miriam-gene:1636
,
lld:C0017665
;
a
sio:SIO_001121
.
}
dgn-np:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_provenance
{
dgn-np:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_assertion
dcterms:description
"[The ACE, AGT, and eNOS genes were correlated with the development of renal function failure in IgAN, whereas the ACE and eNOS genes were associated with the degree of proteinuria and the development of renal function failure in MN.]. 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:24157068
;
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:NP283721.RAxQIL87Al2P2Y-BSkMa7iAItiZkDQzHloXqBY6drK4UU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:40+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" .
}