@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA
> .
@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:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_head
{
this:
np:hasAssertion
dgn-np:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_assertion
;
np:hasProvenance
dgn-np:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_provenance
;
np:hasPublicationInfo
dgn-np:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_assertion
a
np:Assertion
.
dgn-np:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_provenance
a
np:Provenance
.
dgn-np:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_assertion
{
miriam-gene:1017
a
ncit:C16612
.
lld:C0024299
a
ncit:C7057
.
dgn-gda:DGNe49ff4ef3c826f891205323553df9809
sio:SIO_000628
miriam-gene:1017
,
lld:C0024299
;
a
sio:SIO_001121
.
}
dgn-np:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_provenance
{
dgn-np:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_assertion
dcterms:description
"[In this study, we have used YAC probes encompassing the CDKN2 locus to analyze by fluorescence in situ hybridization patients with leukemia and lymphoma and translocations involving 9p in order to establish the CDKN2 status in relation to the karyotype.]. 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:9258663
;
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:NP592856.RANx4bK-rVWbrvSzbx0Ex5TVUlahJNyp3YS0WlDFnGxeA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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" .
}