@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI
> .
@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:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_head
{
this:
np:hasAssertion
dgn-np:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_assertion
;
np:hasProvenance
dgn-np:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_provenance
;
np:hasPublicationInfo
dgn-np:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_assertion
a
np:Assertion
.
dgn-np:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_provenance
a
np:Provenance
.
dgn-np:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_assertion
{
miriam-gene:5879
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN88430405845157461172a5a4d627d91a
sio:SIO_000628
miriam-gene:5879
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_provenance
{
dgn-np:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_assertion
dcterms:description
"[In this study, we demonstrate that unlike oncogenic Ras proteins, which are primarily activated by mutations that eliminate GTPase activity, the activated melanoma RAC1(P29S) protein maintains intrinsic GTP hydrolysis and is spontaneously activated by substantially increased inherent GDP/GTP nucleotide exchange.]. 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:23284172
;
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:NP238591.RAMoznVHoHB7o_9SRkK1bepOBE_TkhN5NKyiH7UIMcbzI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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: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" .
}