@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:8710
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGNe2e3d88d7a3a168bb5e26a642378f343
sio:SIO_000628
miriam-gene:8710
,
lld:C0022661
;
a
sio:SIO_001122
.
}
dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance
{
dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion
dcterms:description
"[We investigated a possible association of two C2093T, C2180T polymorphisms of the megsin gene with the progression of IgAN towards ESRD, as well as the haplotype reconstruction of megsin gene polymorphisms and clinical manifestation of IgAN.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:18498720
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:50+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
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;
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
"v4.0.0.0" .
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"v4.0.0" .
}