@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E
> .
@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:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_head
{
this:
np:hasAssertion
dgn-np:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_assertion
;
np:hasProvenance
dgn-np:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_assertion
a
np:Assertion
.
dgn-np:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_provenance
a
np:Provenance
.
dgn-np:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_assertion
{
miriam-gene:933
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNb95c2504da1310c8b1dc586a8f5317ad
sio:SIO_000628
miriam-gene:933
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_provenance
{
dgn-np:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_assertion
dcterms:description
"[In this study, variation screening of the entire CD22 coding region was performed, and possible association with rheumatic diseases was tested, using the genomic DNA from 207 healthy Japanese individuals, 68 patients with systemic lupus erythematosus (SLE), and 119 patients with rheumatoid arthritis (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:10079291
;
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:NP311822.RASV_KcqoUBxNlh1rRlX0uTY4rbvDntA_kaWcnFQX-F3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}