@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE
> .
@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:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_head
{
this:
np:hasAssertion
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_assertion
;
np:hasProvenance
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_provenance
;
np:hasPublicationInfo
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_assertion
a
np:Assertion
.
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_provenance
a
np:Provenance
.
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_assertion
{
miriam-gene:55907
a
ncit:C16612
.
lld:C0042384
a
ncit:C7057
.
dgn-gda:DGNa0c73a2969801eff8c706f4bbb4d474e
sio:SIO_000628
miriam-gene:55907
,
lld:C0042384
;
a
sio:SIO_001121
.
}
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_provenance
{
dgn-np:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_assertion
dcterms:description
"[CSS has 2 major clinical subsets, antineutrophil cytoplasmic antibody (ANCA)-positive, with features of small-vessel vasculitis, and ANCA-negative, in which organ damage is mainly mediated by tissue eosinophilic infiltration; analysis of HLA-DRB4 in patients categorized by different numbers of vasculitic manifestations (purpura, alveolar hemorrhage, mononeuritis multiplex, rapidly progressive glomerulonephritis, and constitutional symptoms) showed that its frequency strongly correlated with the number of vasculitis symptoms (P for trend = 0.001).]. 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:17763415
;
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:NP301964.RAKvV2TRfWcaT8DYLGx4kpACScyoGoLhcDAVbSftuDLzE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:51+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" .
}