@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk
> .
@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:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_head
{
this:
np:hasAssertion
dgn-np:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_assertion
;
np:hasProvenance
dgn-np:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_provenance
;
np:hasPublicationInfo
dgn-np:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_assertion
a
np:Assertion
.
dgn-np:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_provenance
a
np:Provenance
.
dgn-np:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_assertion
{
miriam-gene:596
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN950a1322d2dbea87008989679fa13eaf
sio:SIO_000628
miriam-gene:596
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_provenance
{
dgn-np:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_assertion
dcterms:description
"[Therefore, we examined 170 cases of B-cell chronic lymphocytic leukemia (B-CLL), 7 cases of B-cell prolymphocytic leukemia (B-PLL), 25 cases of hairy cell leukemia (HCL) and 22 cases of splenic lymphoma with villous lymphocytes (SLVL) with defined cytogenetic abnormalities by DNA blot using both 5' and 3' BCL2 probes to search for rearrangement of the BCL2 locus.]. 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:8204892
;
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:NP305333.RA7X_CfNVjHYKfCk49Tr9cDszza8EtmN0Q-XRid35ZTLk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}