@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A
> .
@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:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_head
{
this:
np:hasAssertion
dgn-np:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_assertion
;
np:hasProvenance
dgn-np:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_assertion
a
np:Assertion
.
dgn-np:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_provenance
a
np:Provenance
.
dgn-np:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0349631
a
ncit:C7057
.
dgn-gda:DGN9d524ba903ef2489578a948b51fae6e6
sio:SIO_000628
miriam-gene:472
,
lld:C0349631
;
a
sio:SIO_001121
.
}
dgn-np:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_provenance
{
dgn-np:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_assertion
dcterms:description
"[Using a laser-capture microdissection we analyzed small and large leukemic bone marrow cells from 19 patients with RS for loss of heterozygosity (LOH) on chromosome 11 (D11S2179 at the ATM gene), 17 (D17S938 and D17S1852 at the TP53 site), and 20 (Plc1, D20S96, D20S110, and D20S119).]. 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:12950231
;
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:NP183738.RAePMrjjAsQHw7gJx8KPUmqN3BbE5nZ_TFooUGts7Hq8A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}