@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo
> .
@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:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_head
{
this:
np:hasAssertion
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_assertion
;
np:hasProvenance
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_assertion
a
np:Assertion
.
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_provenance
a
np:Provenance
.
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_assertion
{
miriam-gene:8036
a
ncit:C16612
.
lld:C0028326
a
ncit:C7057
.
dgn-gda:DGN56cf0ec63f097740648fa55c105d52f7
sio:SIO_000628
miriam-gene:8036
,
lld:C0028326
;
a
sio:SIO_001121
.
}
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_provenance
{
dgn-np:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_assertion
dcterms:description
"[We reported for the first time a case of 13-year-old boy with NS with loose anagen hair (NSLAH) resulting from mutation in SHOC2 who developed an autoimmune disorder that fulfilled four American College of Rheumatology (ACR) criteria for the classification of SLE (polyarthritis, pericarditis, antinuclear antibodies, and anti-DNA antibodies).]. 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:23786871
;
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:NP1087646.RACIcIz4URLd0j_NXEBk6HZOEzLj4P0PaUFd_59Fxl2fo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:59+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" .
}