@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U
> .
@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:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_head
{
this:
np:hasAssertion
dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_assertion
;
np:hasProvenance
dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_provenance
;
np:hasPublicationInfo
dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_assertion
a
np:Assertion
.
dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_provenance
a
np:Provenance
.
dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_assertion
{
miriam-gene:4853
a
ncit:C16612
.
lld:C0009404
a
ncit:C7057
.
dgn-gda:DGNbddb3f4a81e8255b12503b4b14a1cd10
sio:SIO_000628
miriam-gene:4853
,
lld:C0009404
;
a
sio:SIO_001121
.
}
dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_provenance
{
dgn-np:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_assertion
dcterms:description
"[We find large and small chromothripsis events in nearly every colorectal tumor sample and show that several breakpoints of chromothripsis clusters and isolated rearrangements affect cancer genes, including NOTCH2, EXO1 and MLL3.]. 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:22014273
;
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:NP854869.RAREid7-o1imUV7w_TWg0PZVH2TTr1EK8MoSMOOqtkI6U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:43+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" .
}