@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME
> .
@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:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_head
{
this:
np:hasAssertion
dgn-np:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_assertion
;
np:hasProvenance
dgn-np:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_provenance
;
np:hasPublicationInfo
dgn-np:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_assertion
a
np:Assertion
.
dgn-np:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_provenance
a
np:Provenance
.
dgn-np:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_assertion
{
miriam-gene:718
a
ncit:C16612
.
lld:C0017662
a
ncit:C7057
.
dgn-gda:DGN10937522f3d7350a8707f02b73fbd033
sio:SIO_000628
miriam-gene:718
,
lld:C0017662
;
a
sio:SIO_001121
.
}
dgn-np:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_provenance
{
dgn-np:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_assertion
dcterms:description
"[In TTP against ADAMTS 13, the vWF cleaving protease and in the DEAP-HUS (Deficient for CFHR1 and CFHR3 proteins and autoantibody positive) group against the major complement regulator Factor H. Autoantibodies in MPGN are termed C3 Nephritic Factor (C3NeF) and are directed against a neoepitope of the complement C3 convertase C3bBb.]. 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:19640589
;
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:NP481940.RADhLemdNJ_W8GuC8pSrgRCnJVIvdzXQSoGfYwxAcqYME130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}