@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE
> .
@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:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_head
{
this:
np:hasAssertion
dgn-np:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_assertion
;
np:hasProvenance
dgn-np:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_provenance
;
np:hasPublicationInfo
dgn-np:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_assertion
a
np:Assertion
.
dgn-np:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_provenance
a
np:Provenance
.
dgn-np:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_assertion
{
miriam-gene:3127
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN6b22cfd42614a931d35fcdaa764db9e1
sio:SIO_000628
miriam-gene:3127
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_provenance
{
dgn-np:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_assertion
dcterms:description
"[Other research groups, who have shown negative results in studies on affected sibling pairs, have questioned the influence of the HLA class II genes, although they confirmed the association of the DR15,DQ6,Dw2 haplotype to 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:9065561
;
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:NP171074.RARrho-fVm8LeIMhmg-V42eOgT7h4_4-S9AGRJjZRgUNE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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" .
}