@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP96353.RAYPn9cl7qbmY_6Y_PndFS8LXd0YF9LsEFy0LKOl05HQU
> .
@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 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:NP96353.RAYPn9cl7qbmY_6Y_PndFS8LXd0YF9LsEFy0LKOl05HQU130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP96353.RAYPn9cl7qbmY_6Y_PndFS8LXd0YF9LsEFy0LKOl05HQU130_publicationInfo
;
a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP96353.RAYPn9cl7qbmY_6Y_PndFS8LXd0YF9LsEFy0LKOl05HQU130_provenance
a
np:Provenance
.
dgn-np:NP96353.RAYPn9cl7qbmY_6Y_PndFS8LXd0YF9LsEFy0LKOl05HQU130_publicationInfo
a
np:PublicationInfo
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{
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a
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.
lld:C0026769
a
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.
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sio:SIO_000628
miriam-gene:8320
,
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;
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.
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dgn-np:NP96353.RAYPn9cl7qbmY_6Y_PndFS8LXd0YF9LsEFy0LKOl05HQU130_provenance
{
dgn-np:NP96353.RAYPn9cl7qbmY_6Y_PndFS8LXd0YF9LsEFy0LKOl05HQU130_assertion
dc:description
"[We have performed a meta-analysis of GWAS in MS that more than doubles the size of previous gene discovery efforts and highlights 3 novel MS susceptibility loci. These and additional loci with suggestive evidence of association are excellent candidates for further investigations to refine and validate their role in the genetic architecture of MS.]. 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:22190364
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP96353.RAYPn9cl7qbmY_6Y_PndFS8LXd0YF9LsEFy0LKOl05HQU130_publicationInfo
{
this:
dc:created
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xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> ;
pav:createdBy
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pav:version
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