@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_head
{
this:
np:hasAssertion
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_assertion
;
np:hasProvenance
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_provenance
;
np:hasPublicationInfo
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_assertion
a
np:Assertion
.
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_provenance
a
np:Provenance
.
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_assertion
{
miriam-gene:572
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGN4f9ec9e812ac081040a708abfae20211
sio:SIO_000628
miriam-gene:572
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_provenance
{
dgn-np:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_assertion
dcterms:description
"[To explore the possibility that the genetic alterations of Bad might be involved in the development of human cancers, we analyzed the entire coding region and all splice sites of human Bad gene in 47 colon adenocarcinomas.]. 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:15033904
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP258800.RASrWCFmarMP9bxXCWPX5mvCc_WBsXX2VFIxxcbVAUP7g130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:07+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}