@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA
> .
@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/v4.0.0/void/
> .
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_head
{
this:
np:hasAssertion
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_assertion
;
np:hasProvenance
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_provenance
;
np:hasPublicationInfo
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_assertion
a
np:Assertion
.
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_provenance
a
np:Provenance
.
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN697e8390a53240bec392ceb1356ddef6
sio:SIO_000628
miriam-gene:2187
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_provenance
{
dgn-np:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_assertion
dcterms:description
"[Although we confirmed, as usually described, that some recurrent cytogenetic abnormalities are correlated with the FAB subtypes, we noted however that some of them vary in frequency among different geographical areas and ethnic groups.]. 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:22549442
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP978882.RACIbu_jVJxFsM8_C2WXnJyyKsYHTiFf3M3eA6l0egepA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:08+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}