@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0
> .
@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:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_head
{
this:
np:hasAssertion
dgn-np:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_assertion
;
np:hasProvenance
dgn-np:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_provenance
;
np:hasPublicationInfo
dgn-np:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_assertion
a
np:Assertion
.
dgn-np:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_provenance
a
np:Provenance
.
dgn-np:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_assertion
{
miriam-gene:4922
a
ncit:C16612
.
lld:C0035258
a
ncit:C7057
.
dgn-gda:DGN5ed30c20164bd844bbf3f95c5bb809ee
sio:SIO_000628
miriam-gene:4922
,
lld:C0035258
;
a
sio:SIO_001121
.
}
dgn-np:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_provenance
{
dgn-np:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_assertion
dcterms:description
"[The purpose of the current study is to further explore the NTS gene for potential functional variant(s) in its entire genomic and potential regulatory regions and their possible association with RLS symptoms.]. 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:17644423
;
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:NP776000.RALg15H2ZgpiRx2o-gOqAbvMM4llClrNMUmgEexWboIA0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:50+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" .
}