@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1272767.RAJ7Z4kkO7_Ed9Oxv55sKjSSJJoikpDrhVFEUHlDd23fg
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP1272767.RAJ7Z4kkO7_Ed9Oxv55sKjSSJJoikpDrhVFEUHlDd23fg130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1272767.RAJ7Z4kkO7_Ed9Oxv55sKjSSJJoikpDrhVFEUHlDd23fg130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP1272767.RAJ7Z4kkO7_Ed9Oxv55sKjSSJJoikpDrhVFEUHlDd23fg130_provenance
a
np:Provenance
.
dgn-np:NP1272767.RAJ7Z4kkO7_Ed9Oxv55sKjSSJJoikpDrhVFEUHlDd23fg130_publicationInfo
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.
}
dgn-np:NP1272767.RAJ7Z4kkO7_Ed9Oxv55sKjSSJJoikpDrhVFEUHlDd23fg130_assertion
{
miriam-gene:23019
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN12ce8b5d5c20022e5b755ad87fb7504d
sio:SIO_000628
miriam-gene:23019
,
lld:C0023434
;
a
sio:SIO_001122
.
}
dgn-np:NP1272767.RAJ7Z4kkO7_Ed9Oxv55sKjSSJJoikpDrhVFEUHlDd23fg130_provenance
{
dgn-np:NP1272767.RAJ7Z4kkO7_Ed9Oxv55sKjSSJJoikpDrhVFEUHlDd23fg130_assertion
dcterms:description
"[We found nine statistically significant associations with CLL risk after FDR correction, seven in miRNA processing genes (rs3805500 and rs6877842 in DROSHA, rs1057035 in DICER1, rs17676986 in SND1, rs9611280 in TNRC6B, rs784567 in TRBP and rs11866002 in CNOT1) and two in pre-miRNAs (rs11614913 in miR196a2 and rs2114358 in miR1206).]. 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:25793711
;
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:NP1272767.RAJ7Z4kkO7_Ed9Oxv55sKjSSJJoikpDrhVFEUHlDd23fg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:23+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
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;
pav:authoredBy
<
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> , <
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
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pav:version
"v4.0.0" .
}