@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0
> .
@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:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_head
{
this:
np:hasAssertion
dgn-np:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_assertion
;
np:hasProvenance
dgn-np:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_provenance
;
np:hasPublicationInfo
dgn-np:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_assertion
a
np:Assertion
.
dgn-np:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_provenance
a
np:Provenance
.
dgn-np:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGN5dbff0328a4713365dd0e1ff9a5d5d38
sio:SIO_000628
miriam-gene:1030
,
lld:C1961102
;
a
sio:SIO_001121
.
}
dgn-np:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_provenance
{
dgn-np:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_assertion
dcterms:description
"[The data presented in this report showed that (1) p16INK4A and p15INK4B genes are preferentially deleted homozygously in ALL and heterozygously in CLL cases with frequent mutation in the second allele, and (2) p16INK4A gene appears to be more frequently deleted than p15INK4B gene.]. 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:7795238
;
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:NP427951.RANWXT6rNr0HnJPMvAqR5FzHyOpwcengbvrb9aWir-TJ0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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" .
}