@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0
> .
@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:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_head
{
this:
np:hasAssertion
dgn-np:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_assertion
;
np:hasProvenance
dgn-np:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance
;
np:hasPublicationInfo
dgn-np:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_assertion
a
np:Assertion
.
dgn-np:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance
a
np:Provenance
.
dgn-np:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_assertion
{
miriam-gene:6556
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN2937ebad8ac5fb4f12ff63fc7c2ea90e
sio:SIO_000628
miriam-gene:6556
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_provenance
{
dgn-np:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_assertion
dcterms:description
"[In view of the emerging role of polymorphic variants in complex diseases and minimizing of possible confounding factors in this association study, we conclude that allelic variation in the NRAMP1 promoter may contribute significantly to MS susceptibility in the South African Caucasian population.]. 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:11358358
;
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:NP194414.RAYU9O9EqwMoYJEMhBC8MNejnzb9obSMMzaQ5Z6vBz6K0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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
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"v2.1.0" .
}