@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA
> .
@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:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_head
{
this:
np:hasAssertion
dgn-np:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_assertion
;
np:hasProvenance
dgn-np:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_provenance
;
np:hasPublicationInfo
dgn-np:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_assertion
a
np:Assertion
.
dgn-np:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_provenance
a
np:Provenance
.
dgn-np:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_assertion
{
miriam-gene:2475
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN528864bc19e8581ff4c8ae83ed677a3e
sio:SIO_000628
miriam-gene:2475
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_provenance
{
dgn-np:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_assertion
dcterms:description
"[To determine whether genetic variations in mTOR are associated with risk of acute lymphoblastic leukemia (ALL) in Chinese children, we genotyped two tag single nucleotide poymorphisms (SNPs) in mTOR (rs2536 and rs2295080) in a case-control study.]. 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:21973240
;
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:NP827739.RAnqY7GOQ_PRc2BRmSr6jrRNQrThHyj8vjZ-IaG0AYqeA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:26+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" .
}