@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA
> .
@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/v3.0.0/void/
> .
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_head
{
this:
np:hasAssertion
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_assertion
;
np:hasProvenance
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_provenance
;
np:hasPublicationInfo
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_assertion
a
np:Assertion
.
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_provenance
a
np:Provenance
.
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0039082
a
ncit:C7057
.
dgn-gda:DGN600552c5d6257412910b93f5b6a6904d
sio:SIO_000628
miriam-gene:64127
,
lld:C0039082
;
a
sio:SIO_001122
.
}
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_provenance
{
dgn-np:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_assertion
dcterms:description
"[Danish sarcoidosis patients have frequent variations in CARD15 exon 4, but do not present any mutation associated with Blau syndrome. The variations found had no influence on the course of disease.]. 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:20298285
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP102362.RAq_f4m-kLDC6flAwiQ340aN3Hem1fOCQp5dyMNPxbyYA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:36+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}