@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc
> .
@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:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_head
{
this:
np:hasAssertion
dgn-np:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_assertion
;
np:hasProvenance
dgn-np:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_provenance
;
np:hasPublicationInfo
dgn-np:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_assertion
a
np:Assertion
.
dgn-np:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_provenance
a
np:Provenance
.
dgn-np:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_assertion
{
miriam-gene:5602
a
ncit:C16612
.
lld:C0006118
a
ncit:C7057
.
dgn-gda:DGNf02c930f7f0e7ccc1359f6cad984ee09
sio:SIO_000628
miriam-gene:5602
,
lld:C0006118
;
a
sio:SIO_001121
.
}
dgn-np:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_provenance
{
dgn-np:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_assertion
dcterms:description
"[Together with prior evidence that, in JNK3-deficient mice, the JNK3 signaling pathway mediates apoptosis in central nervous tissue, our results suggest that loss of expression of the JNK3 gene may play an important role in the development of brain tumors in humans.]. 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:11322657
;
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:NP775365.RAppuDjqmEuxFuIFiJWDSQ-1u8zmGlCt1bg5DgTREkOgc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:49+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" .
}