@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI
> .
@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:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_head
{
this:
np:hasAssertion
dgn-np:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_assertion
;
np:hasProvenance
dgn-np:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_provenance
;
np:hasPublicationInfo
dgn-np:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_assertion
a
np:Assertion
.
dgn-np:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_provenance
a
np:Provenance
.
dgn-np:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN60a5b2a9c38119e3a7eb1b56ae19a9d6
sio:SIO_000628
miriam-gene:3342
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_provenance
{
dgn-np:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_assertion
dcterms:description
"[In this study, we describe the application of comparative genomic hybridization (CGH) to investigate the genomic abnormalities in 14 patients with ALL, all of whom had cytogenetically identified numerical aberrations or gross chromosomal structural alteration.]. 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:9595040
;
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:NP731864.RAJaB0sCSfGfsen43fW_eAF6d6vA2fjlan49zZw45uJTI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:24+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" .
}