@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4
> .
@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:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_head
{
this:
np:hasAssertion
dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_assertion
;
np:hasProvenance
dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_provenance
;
np:hasPublicationInfo
dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_assertion
a
np:Assertion
.
dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_provenance
a
np:Provenance
.
dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_assertion
{
miriam-gene:4170
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN05a7deb510a2c506283e1224aec74119
sio:SIO_000628
miriam-gene:4170
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_provenance
{
dgn-np:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_assertion
dcterms:description
"[A common insertional polymorphism in promoter of MCL1, a member of BCL2 family gene with the dual regulatory functions, has been shown to be functional in leukemia, but its association with cancer predisposition and prognosis has not been well established.]. 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:21887682
;
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:NP168481.RADhWPHRSkviESxBOTZhZbmudtPf7Xv5A8Kz6UpjP_7V4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}