@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc
> .
@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:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_head
{
this:
np:hasAssertion
dgn-np:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_assertion
;
np:hasProvenance
dgn-np:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_provenance
;
np:hasPublicationInfo
dgn-np:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_assertion
a
np:Assertion
.
dgn-np:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_provenance
a
np:Provenance
.
dgn-np:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_assertion
{
miriam-gene:9271
a
ncit:C16612
.
lld:C0278996
a
ncit:C7057
.
dgn-gda:DGN290499b4aa0d4c7fec1738a11f42d93a
sio:SIO_000628
miriam-gene:9271
,
lld:C0278996
;
a
sio:SIO_001121
.
}
dgn-np:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_provenance
{
dgn-np:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_assertion
dcterms:description
"[To test this hypothesis, we genotyped three SNPs at miRNA binding sites of miRNA processing genes (rs1057035 in 3'UTR of DICER, rs3803012 in 3'UTR of RAN and rs10773771 in 3'UTR of HIWI) with a case-control study including 397 HNC cases and 900 controls matched by age and sex in Chinese.]. 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:23071822
;
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:NP599221.RAphGlqBkoRffYe4-FVL0yJe8H3CdOxjv_SE-CDujV0yc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}