@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM
> .
@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:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_head
{
this:
np:hasAssertion
dgn-np:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_assertion
;
np:hasProvenance
dgn-np:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_provenance
;
np:hasPublicationInfo
dgn-np:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_assertion
a
np:Assertion
.
dgn-np:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_provenance
a
np:Provenance
.
dgn-np:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0011603
a
ncit:C7057
.
dgn-gda:DGNa670f8473e7b3b66e9a0fdbf3c22ecb9
sio:SIO_000628
miriam-gene:64127
,
lld:C0011603
;
a
sio:SIO_001121
.
}
dgn-np:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_provenance
{
dgn-np:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_assertion
dcterms:description
"[Blau's syndrome (familial juvenile systemic granulomatosis) presents with non-caseating granulomatous inflammation affecting the joint, skin, and uveal tract (the triad of arthritis, dermatitis and uveitis) and is associated with mutations of the NACHT domain of the gene CARD15 (or NOD2).]. 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:22714396
;
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:NP600211.RAyc2XP-6pZEtxVesNaB-BgdeJoDDyaPvGIBpVtZlrOEM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}