@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU
> .
@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:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_head
{
this:
np:hasAssertion
dgn-np:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_assertion
;
np:hasProvenance
dgn-np:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_provenance
;
np:hasPublicationInfo
dgn-np:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_assertion
a
np:Assertion
.
dgn-np:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_provenance
a
np:Provenance
.
dgn-np:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_assertion
{
miriam-gene:4515
a
ncit:C16612
.
lld:C0242621
a
ncit:C7057
.
dgn-gda:DGNbc2ef1906674bf3dcc92957284077560
sio:SIO_000628
miriam-gene:4515
,
lld:C0242621
;
a
sio:SIO_001121
.
}
dgn-np:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_provenance
{
dgn-np:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_assertion
dcterms:description
"[Previous cytogenetic and molecular studies reported complex karyotypes with recurrent chromosomal abnormalities, including translocations involving either TCL1 at 14q32.1 or MTCP1 at Xq28, inactivation of the ATM gene by deletion and/or mutation, and isochromosomes 8.]. 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:11391795
;
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:NP574093.RAvQZdUz8kBfYpgVHPBE2nnyzD2KrM7-QfqTTpIgCKnIU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:22+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" .
}