@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs
> .
@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:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_head
{
this:
np:hasAssertion
dgn-np:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_assertion
;
np:hasProvenance
dgn-np:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_provenance
;
np:hasPublicationInfo
dgn-np:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_assertion
a
np:Assertion
.
dgn-np:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_provenance
a
np:Provenance
.
dgn-np:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN9c29ed6f5016ab69f23a37471f33dc09
sio:SIO_000628
miriam-gene:7248
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_provenance
{
dgn-np:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_assertion
dcterms:description
"[Abnormalities at 13q, though not correlated with particular clinical syndromes, are the subject of intense interest due to the possibility that one or more tumour suppressor genes relevant to the pathogenesis of CLL may be identified.]. 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:9471056
;
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:NP404824.RAGmV99qUJ5_RDlOLlceC_iLBOQFntD7tw6BgR8ElWyKs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:01+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" .
}