@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY
> .
@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:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_head
{
this:
np:hasAssertion
dgn-np:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_assertion
;
np:hasProvenance
dgn-np:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_provenance
;
np:hasPublicationInfo
dgn-np:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_assertion
a
np:Assertion
.
dgn-np:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_provenance
a
np:Provenance
.
dgn-np:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN94977958be5d27b342989d20b2024ced
sio:SIO_000628
miriam-gene:1029
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_provenance
{
dgn-np:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_assertion
dcterms:description
"[We analyzed p16INK4A and p15INK4B genes in 178 cases of primary leukemias including 81 cases of chronic lymphocytic leukemia (CLL), seven of hairy cell leukemia (HCL), seven of chronic myelogenous leukemia (CML), 43 of acute myelogenous leukemia (AML), 27 of acute lymphoblastic leukemia (ALL), and 13 of myelodysplastic syndrome (MDS) by Southern blot analyses.]. 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:7795238
;
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:NP801505.RAOQ-zHatzH9HrtRTiPlsscbFGTB78e7sTT1iPyMFJ7SY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:12+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" .
}