@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_assertion
;
np:hasProvenance
dgn-np:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_provenance
;
np:hasPublicationInfo
dgn-np:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_assertion
a
np:Assertion
.
dgn-np:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_provenance
a
np:Provenance
.
dgn-np:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_assertion
{
miriam-gene:28514
a
ncit:C16612
.
lld:C0023290
a
ncit:C7057
.
dgn-gda:DGN080647f285a1fb064effd08459599fee
sio:SIO_000628
miriam-gene:28514
,
lld:C0023290
;
a
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.
}
dgn-np:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_provenance
{
dgn-np:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_assertion
dcterms:description
"[This well-powered genetic and functional study in an Indian population provides evidence supporting DLL1 as the etiological gene contributing to susceptibility to VL at Chromosome 6q27, confirming the potential for polymorphism at DLL1 to act as a genetic risk factor across the epidemiological divides of geography and parasite species.]. 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:22561395
;
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:NP654794.RAsoGq3CLI3-j5wuTfUO8za3A9N5vh2D-hU-r9DSnt68A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:34+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" .
}