@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I
> .
@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:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_head
{
this:
np:hasAssertion
dgn-np:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_assertion
;
np:hasProvenance
dgn-np:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_provenance
;
np:hasPublicationInfo
dgn-np:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_assertion
a
np:Assertion
.
dgn-np:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_provenance
a
np:Provenance
.
dgn-np:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_assertion
{
miriam-gene:3315
a
ncit:C16612
.
lld:C3489791
a
ncit:C7057
.
dgn-gda:DGN1ea7fd6aae50debb2c6c8d1013c938fa
sio:SIO_000628
miriam-gene:3315
,
lld:C3489791
;
a
sio:SIO_001121
.
}
dgn-np:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_provenance
{
dgn-np:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_assertion
dcterms:description
"[We therefore compared total levels and activation of the signalling proteins Src, HSP27, p38 MAPK, JNK, and ERK, in extracts of leukocytes isolated from patients with PD carrying the G2019S mutation, healthy mutation carriers, patients with idiopathic PD, and healthy controls.]. 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:17385669
;
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:NP571419.RAEyZD8ydUFLkgEjzWMhpmceKgVtBaYkaVS8TExYnu01I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:44+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" .
}