@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM
> .
@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:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_head
{
this:
np:hasAssertion
dgn-np:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_assertion
;
np:hasProvenance
dgn-np:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_provenance
;
np:hasPublicationInfo
dgn-np:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_assertion
a
np:Assertion
.
dgn-np:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_provenance
a
np:Provenance
.
dgn-np:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_assertion
{
miriam-gene:4297
a
ncit:C16612
.
lld:C0751606
a
ncit:C7057
.
dgn-gda:DGN7463e18591591574feaea61259bf3b4d
sio:SIO_000628
miriam-gene:4297
,
lld:C0751606
;
a
sio:SIO_001121
.
}
dgn-np:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_provenance
{
dgn-np:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_assertion
dcterms:description
"[The relatively high frequency of deletion of the D11S2179 marker compared with the D11S1356 marker suggests that ATM is the target gene of the deletion at the 11q23 locus, and that such deletions may play a role in the pathogenesis of ALL.]. 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:10699895
;
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:NP559271.RAc6RF9_8fByvlH7UQGTwXLHHdEtJGNqG3NnlTvMT5TSM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:12+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" .
}