@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI
> .
@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:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_head
{
this:
np:hasAssertion
dgn-np:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_assertion
;
np:hasProvenance
dgn-np:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_provenance
;
np:hasPublicationInfo
dgn-np:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_assertion
a
np:Assertion
.
dgn-np:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_provenance
a
np:Provenance
.
dgn-np:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_assertion
{
miriam-gene:7190
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN4065cb529ab9aca92955d19876d73fc7
sio:SIO_000628
miriam-gene:7190
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_provenance
{
dgn-np:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_assertion
dcterms:description
"[When constitutional symptoms such as myalgia, weight loss, fatigue, fever, and hypertension were added to the clinical picture, the diagnosis of polyarteritis nodosa HSP was thought and confirmed by the demonstration of microaneurisms on renal arteries.]. 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:21259007
;
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:NP163506.RAFaDkUsUHPa23YOmfS859WW3Pe8s75bDpv0RJtDzs8MI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}