@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE
> .
@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:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_head
{
this:
np:hasAssertion
dgn-np:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_assertion
;
np:hasProvenance
dgn-np:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_provenance
;
np:hasPublicationInfo
dgn-np:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_assertion
a
np:Assertion
.
dgn-np:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_provenance
a
np:Provenance
.
dgn-np:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0376545
a
ncit:C7057
.
dgn-gda:DGNda9c96d77004fffc7faf111685649b5a
sio:SIO_000628
miriam-gene:1029
,
lld:C0376545
;
a
sio:SIO_001121
.
}
dgn-np:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_provenance
{
dgn-np:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_assertion
dcterms:description
"[Remarkably distinct patterns of inactivation of p15INK4B and p16INK4A characterize different types of hematological malignancy, and alterations in these tumor suppressor genes are one of the most common alterations in hematological malignancies.]. 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:9041182
;
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:NP553348.RAdhuzwXywtXt839MHpOAEVwjmezWX7ps5mbRLr5LXHTE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}