@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY
> .
@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:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_head
{
this:
np:hasAssertion
dgn-np:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_assertion
;
np:hasProvenance
dgn-np:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_provenance
;
np:hasPublicationInfo
dgn-np:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_assertion
a
np:Assertion
.
dgn-np:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_provenance
a
np:Provenance
.
dgn-np:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_assertion
{
miriam-gene:930
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN9e56f75faa3ccfafba206d26718b4975
sio:SIO_000628
miriam-gene:930
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_provenance
{
dgn-np:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_assertion
dcterms:description
"[To assess the impact of somatic hypermutation and selective influences on the Vlambda light chain repertoire in systemic lupus erythematosus (SLE), the frequency and pattern of mutations were analyzed in individual CD19+ B cells from a patient with previously undiagnosed SLE.]. 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:11714391
;
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:NP545843.RAfaO5S41ZMon6l_HuWXn68JPvCpAA-40vqJ0tWZdQfBY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:29+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" .
}