@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_head
{
this:
np:hasAssertion
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_assertion
;
np:hasProvenance
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance
;
np:hasPublicationInfo
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_assertion
a
np:Assertion
.
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance
a
np:Provenance
.
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_assertion
{
miriam-gene:4851
a
ncit:C16612
.
lld:C0152096
a
ncit:C7057
.
dgn-gda:DGNfa383a4ce0e34304c7bcecd35d74152d
sio:SIO_000628
miriam-gene:4851
,
lld:C0152096
;
a
sio:SIO_001121
.
}
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_provenance
{
dgn-np:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_assertion
dcterms:description
"[These findings indicate that the distribution of NOTCH1 mutations in CLL with trisomy 12 is heterogeneous and that the presence of additional chromosomal abnormalities such as trisomy 18 could change the prognosis of these patients.]. 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:22619094
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP595415.RAReD9xj8pR69_BsKxA1lYQpDVcnNmCIvRqeVhbSbyDQY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:36+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}