@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew
> .
@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:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_head
{
this:
np:hasAssertion
dgn-np:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_assertion
;
np:hasProvenance
dgn-np:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_provenance
;
np:hasPublicationInfo
dgn-np:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_assertion
a
np:Assertion
.
dgn-np:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_provenance
a
np:Provenance
.
dgn-np:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_assertion
{
miriam-gene:3133
a
ncit:C16612
.
lld:C0409651
a
ncit:C7057
.
dgn-gda:DGN5c30ce1c559f8c1dd204b4470cde9c47
sio:SIO_000628
miriam-gene:3133
,
lld:C0409651
;
a
sio:SIO_001121
.
}
dgn-np:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_provenance
{
dgn-np:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_assertion
dcterms:description
"[These findings, and particularly the newly recognized association with DRw6, support the hypothesis that functionally equivalent shared epitopes or conformations on otherwise distinct MHC molecules may confer risk for developing RA.]. 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:2259843
;
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:NP748439.RARBO5QIxNxi4M1ww8nxUkQNPJPXtlN4AfnY0CBKMOGew130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}