@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc
> .
@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:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_head
{
this:
np:hasAssertion
dgn-np:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_assertion
;
np:hasProvenance
dgn-np:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_provenance
;
np:hasPublicationInfo
dgn-np:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_assertion
a
np:Assertion
.
dgn-np:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_provenance
a
np:Provenance
.
dgn-np:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_assertion
{
miriam-gene:5870
a
ncit:C16612
.
lld:C0021051
a
ncit:C7057
.
dgn-gda:DGNc55ea48d9283f80f9f369ca236b21ce7
sio:SIO_000628
miriam-gene:5870
,
lld:C0021051
;
a
sio:SIO_001121
.
}
dgn-np:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_provenance
{
dgn-np:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_assertion
dcterms:description
"[In the last decade, the number of genetic diseases driven by germline mutations in Rab GTPases or their interacting proteins, has increased and there is growing evidence of aberrant Rab GTPase function in acquired pathophysiologies such as immune deficiency, infection, obesity, diabetes and cancer.]. 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:21147240
;
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:NP858053.RAOmVNn_7-qP5ph1IZ3vWKnPJG5pQjyurqIHOjm4I86Gc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:13+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" .
}