@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg
> .
@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:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_head
{
this:
np:hasAssertion
dgn-np:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_assertion
;
np:hasProvenance
dgn-np:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_assertion
a
np:Assertion
.
dgn-np:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_provenance
a
np:Provenance
.
dgn-np:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C0268743
a
ncit:C7057
.
dgn-gda:DGNddfd2e885d4e4fe152423483afc7b3b9
sio:SIO_000628
miriam-gene:3075
,
lld:C0268743
;
a
sio:SIO_001121
.
}
dgn-np:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_provenance
{
dgn-np:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_assertion
dcterms:description
"[Dense deposit disease (DDD) is a rare renal disease related to the dysregulation of the alternative pathway of the complement cascade, caused by several factors including the presence of an autoantibody to C3 nephritic factor, mutations in factor H and autoantibodies to this protein.]. 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:24338037
;
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:NP1136952.RAPLxiu3kgH3kYkLLyJu5n1EGsSrrbykZQWcuoMhEBJdg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:21+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}