@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks
> .
@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:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_head
{
this:
np:hasAssertion
dgn-np:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_assertion
;
np:hasProvenance
dgn-np:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_provenance
;
np:hasPublicationInfo
dgn-np:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_assertion
a
np:Assertion
.
dgn-np:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_provenance
a
np:Provenance
.
dgn-np:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_assertion
{
miriam-gene:1154
a
ncit:C16612
.
lld:C0079744
a
ncit:C7057
.
dgn-gda:DGN30e94bced37def06ac7133d588473d24
sio:SIO_000628
miriam-gene:1154
,
lld:C0079744
;
a
sio:SIO_001121
.
}
dgn-np:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_provenance
{
dgn-np:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_assertion
dcterms:description
"[We recently described a colorimetric in situ hybridization (CISH) method for detecting extra copies of the MYC gene in DLBCL and the frequent occurrence of excess copies of discrete MYC signals in the context of diploidy or polyploidy of chromosome 8, which correlated with increased mRNA signals.]. 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:23355209
;
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:NP768891.RAqRLm32webWlqnawm5kaSDL6RuE7R1k5HU-b0Ae459Ks130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+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" .
}