@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI
> .
@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:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_head
{
this:
np:hasAssertion
dgn-np:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_assertion
;
np:hasProvenance
dgn-np:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_provenance
;
np:hasPublicationInfo
dgn-np:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_assertion
a
np:Assertion
.
dgn-np:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_provenance
a
np:Provenance
.
dgn-np:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_assertion
{
miriam-gene:5921
a
ncit:C16612
.
lld:C0028860
a
ncit:C7057
.
dgn-gda:DGNfc914ea88da698f2ffbc6477d21ae452
sio:SIO_000628
miriam-gene:5921
,
lld:C0028860
;
a
sio:SIO_001121
.
}
dgn-np:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_provenance
{
dgn-np:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_assertion
dcterms:description
"[The OCRL1 RhoGAP domain showed low Rac GAP activity in vitro, and when expressed in Swiss 3T3 cells induced specific inhibition of RacGTP dependent ruffles, consistent with OCRL1 being an active RacGAP.]. 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:12915445
;
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:NP800946.RAdxqqK04rGXboiEfjJft7QkNCsjiGSQAOewWEW00HqRI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}