@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g
> .
@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:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_head
{
this:
np:hasAssertion
dgn-np:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_assertion
;
np:hasProvenance
dgn-np:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_provenance
;
np:hasPublicationInfo
dgn-np:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_assertion
a
np:Assertion
.
dgn-np:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_provenance
a
np:Provenance
.
dgn-np:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_assertion
{
miriam-gene:55133
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN5a64458fcd461d42e052af4c25a76436
sio:SIO_000628
miriam-gene:55133
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_provenance
{
dgn-np:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_assertion
dcterms:description
"[Because SRBD1 and ELOVL5 are reportedly involved in the induction of cell growth inhibition or apoptosis, the regulation of SRBD1 and ELOVL5 cascades may play an important physiologic role in the risk of NTG development.]. 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:20363506
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP95088.RAKAFtbbrzX02emrnLT492uIkKycrrlubFtCFJGD3p39g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:47+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" .
}