@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA
> .
@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:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_assertion
;
np:hasProvenance
dgn-np:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_provenance
;
np:hasPublicationInfo
dgn-np:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_assertion
a
np:Assertion
.
dgn-np:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_provenance
a
np:Provenance
.
dgn-np:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_assertion
{
miriam-gene:3123
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGNeb901c426c1ca021a9f5b52ff2558ac0
sio:SIO_000628
miriam-gene:3123
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_provenance
{
dgn-np:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_assertion
dcterms:description
"[These results contribute substantially to our understanding of the DRB1 locus and MS, and underscore the importance of using large sample sizes to detect modest genetic effects, particularly in studies of genotype-phenotype relationships.]. 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:16905561
;
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:NP211777.RApzOEVIjYmaKRrNkHgyDC0O0-2PEwkc0SHFUs39KwZzA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:56+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" .
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