@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY
> .
@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:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_head
{
this:
np:hasAssertion
dgn-np:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_assertion
;
np:hasProvenance
dgn-np:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_provenance
;
np:hasPublicationInfo
dgn-np:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_assertion
a
np:Assertion
.
dgn-np:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_provenance
a
np:Provenance
.
dgn-np:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN049dc8047b9a73c0f5038cb91d00bb5c
sio:SIO_000628
miriam-gene:3126
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_provenance
{
dgn-np:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_assertion
dcterms:description
"[To our knowledge, this is one of the most dramatic examples of genetic disease suppression in individuals who already have developed autoantibodies and of novel dominant suppression of an autoimmune disease by a class I HLA allele.]. 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:21565792
;
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:NP268761.RA9LNisms-bdxyJWifyvFRTBdy2gpa0-e196-tfg6pkzY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:30+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" .
}