@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y
> .
@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:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_head
{
this:
np:hasAssertion
dgn-np:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_assertion
;
np:hasProvenance
dgn-np:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_assertion
a
np:Assertion
.
dgn-np:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_provenance
a
np:Provenance
.
dgn-np:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_assertion
{
miriam-gene:7965
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN7204d6219369a6d00e42cbeab3c03f41
sio:SIO_000628
miriam-gene:7965
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_provenance
{
dgn-np:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_assertion
dcterms:description
"[Strategies merging functional genomic technologies are outlined for the identification of novel posttranscriptionally regulated targets of p38 to show that they are functionally linked to the induction or interruption of cellular growth in 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:18217689
;
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:NP606332.RAd0-RByiYZdESCYO03DBNBvMSuJyfj2t1s3Ugh9jVI2Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}