@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP240376.RAbnU_AAZYgoUaXHIWBCosfBjqU3E3JergL3AmqHLIcSY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP240376.RAbnU_AAZYgoUaXHIWBCosfBjqU3E3JergL3AmqHLIcSY130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP240376.RAbnU_AAZYgoUaXHIWBCosfBjqU3E3JergL3AmqHLIcSY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP240376.RAbnU_AAZYgoUaXHIWBCosfBjqU3E3JergL3AmqHLIcSY130_assertion
a
np:Assertion
.
dgn-np:NP240376.RAbnU_AAZYgoUaXHIWBCosfBjqU3E3JergL3AmqHLIcSY130_provenance
a
np:Provenance
.
dgn-np:NP240376.RAbnU_AAZYgoUaXHIWBCosfBjqU3E3JergL3AmqHLIcSY130_publicationInfo
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{
miriam-gene:3342
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN3bf134b4f235d6d274166f040334c65b
sio:SIO_000628
miriam-gene:3342
,
lld:C0027651
;
a
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.
}
dgn-np:NP240376.RAbnU_AAZYgoUaXHIWBCosfBjqU3E3JergL3AmqHLIcSY130_provenance
{
dgn-np:NP240376.RAbnU_AAZYgoUaXHIWBCosfBjqU3E3JergL3AmqHLIcSY130_assertion
dcterms:description
"[To map the breakpoints more precisely, we constructed a tiling-path matrix-CGH array covering chromosomal band 17p11.2 to the centromere and utilized it to delineate two small breakpoint intervals mapping at Mb 19.0 and 21.7 in seven of the medulloblastomas and in nine hematological neoplasias with i(17q).]. 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:16419060
;
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:NP240376.RAbnU_AAZYgoUaXHIWBCosfBjqU3E3JergL3AmqHLIcSY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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
<
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> , <
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> , <
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
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