@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4
> .
@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:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_head
{
this:
np:hasAssertion
dgn-np:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_assertion
;
np:hasProvenance
dgn-np:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_provenance
;
np:hasPublicationInfo
dgn-np:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_assertion
a
np:Assertion
.
dgn-np:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_provenance
a
np:Provenance
.
dgn-np:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_assertion
{
miriam-gene:129831
a
ncit:C16612
.
lld:C0035450
a
ncit:C7057
.
dgn-gda:DGNe399048b684e3880af4c9a5d93e7fd3f
sio:SIO_000628
miriam-gene:129831
,
lld:C0035450
;
a
sio:SIO_001121
.
}
dgn-np:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_provenance
{
dgn-np:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_assertion
dcterms:description
"[Not all shared epitope DRB1 genotypes conferred the same relative risk, and the male RA group tended to have more compound heterozygous genotypes and more severe RA as indicated by rheumatoid nodules and SAARD usage.]. 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:10332964
;
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:NP692141.RAb5x2qkk3iKccqAHfafJUCO9sFN72HXWjvJ6DQ-63kO4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}