@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc
> .
@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:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_head
{
this:
np:hasAssertion
dgn-np:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_assertion
;
np:hasProvenance
dgn-np:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_provenance
;
np:hasPublicationInfo
dgn-np:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_assertion
a
np:Assertion
.
dgn-np:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_provenance
a
np:Provenance
.
dgn-np:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0017661
a
ncit:C7057
.
dgn-gda:DGNdc296022cf6a625d6ac0fa4807954585
sio:SIO_000628
miriam-gene:8170
,
lld:C0017661
;
a
sio:SIO_001121
.
}
dgn-np:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_provenance
{
dgn-np:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_assertion
dcterms:description
"[In the present study, we evaluated the influence of the C2093T and C2180T polymorphism within the 3' untranslated region (3'UTR) of megsin gene and its haplotypes on the development and progression of Korean IgAN 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:18793525
;
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:NP383906.RAu2ncklzWwKymRJwcaKDHQtB2z58tbA7BgaH2ejCtwlc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:48+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" .
}