@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA
> .
@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:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_head
{
this:
np:hasAssertion
dgn-np:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_assertion
;
np:hasProvenance
dgn-np:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_provenance
;
np:hasPublicationInfo
dgn-np:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_assertion
a
np:Assertion
.
dgn-np:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_provenance
a
np:Provenance
.
dgn-np:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_assertion
{
miriam-gene:5873
a
ncit:C16612
.
lld:C0850497
a
ncit:C7057
.
dgn-gda:DGNa3261443834df7c999ecd45d9b88ef7c
sio:SIO_000628
miriam-gene:5873
,
lld:C0850497
;
a
sio:SIO_001121
.
}
dgn-np:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_provenance
{
dgn-np:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_assertion
dcterms:description
"[Rab27a plays a pivotal role in the transport of melanosomes to dendrite tips of melanocytes and mutations in RAB27A, which impair melanosome transport cause the pigmentary dilution and the immune deficiency found in several patients with Griscelli syndrome (GS).]. 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:12531900
;
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:NP677039.RA74ZKw6gXvGA6OgcnMy-Q_15-mxguVoU4ADv8-0yfNnA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}