@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y
> .
@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:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_head
{
this:
np:hasAssertion
dgn-np:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_assertion
;
np:hasProvenance
dgn-np:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_assertion
a
np:Assertion
.
dgn-np:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_provenance
a
np:Provenance
.
dgn-np:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_assertion
{
miriam-gene:100293534
a
ncit:C16612
.
lld:C0017658
a
ncit:C7057
.
dgn-gda:DGNfe20c34fb420ea7fc75e9d9e3a34a697
sio:SIO_000628
miriam-gene:100293534
,
lld:C0017658
;
a
sio:SIO_001121
.
}
dgn-np:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_provenance
{
dgn-np:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_assertion
dcterms:description
"[The relationship between complete deficiency for either isotype of the fourth component of complement, C4A or C4B, and glomerulonephritis was initially examined in white patients from Kentucky with either IgA nephropathy or Schönlein-Henoch purpura.]. 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:2329414
;
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:NP533271.RA38UxRPTYD_QRjfo977EcFYFX9wXKIlbnrWtDe-Dsu9Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}