@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms
> .
@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:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_head
{
this:
np:hasAssertion
dgn-np:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_assertion
;
np:hasProvenance
dgn-np:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_provenance
;
np:hasPublicationInfo
dgn-np:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_assertion
a
np:Assertion
.
dgn-np:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_provenance
a
np:Provenance
.
dgn-np:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_assertion
{
miriam-gene:4193
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGNa3688eca866729a4d12ade9d038e652f
sio:SIO_000628
miriam-gene:4193
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_provenance
{
dgn-np:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_assertion
dcterms:description
"[Since trisomy 12 is the most common chromosome abnormality found in CLL and MDM2 has been mapped to this chromosome, we examined the possible association of MDM2 in the pathogenesis of CLL.]. 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:8092130
;
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:NP488036.RAYzmGwhe4wVNAnuqU9WtM7kpBO8b1E0NxNgnmq_-G6Ms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}