@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY
> .
@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:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_head
{
this:
np:hasAssertion
dgn-np:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_assertion
;
np:hasProvenance
dgn-np:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_provenance
;
np:hasPublicationInfo
dgn-np:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_assertion
a
np:Assertion
.
dgn-np:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_provenance
a
np:Provenance
.
dgn-np:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_assertion
{
miriam-gene:54474
a
ncit:C16612
.
lld:C0242596
a
ncit:C7057
.
dgn-gda:DGN71f9247da95814340aa6606c9bc50c16
sio:SIO_000628
miriam-gene:54474
,
lld:C0242596
;
a
sio:SIO_001121
.
}
dgn-np:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_provenance
{
dgn-np:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_assertion
dcterms:description
"[A preferred panel would also include CD20, CD117, CD28 and CD27; 4) discrepancies between the percentage of plasma cells detected by flow cytometry and morphology are primarily related to sample quality and it is, therefore, important to determine that marrow elements are present in follow-up samples, particularly normal plasma cells in MRD negative cases.]. 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:18268286
;
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:NP371331.RAH9FVEhtYkHLrTL_XoJ9OgyeajUoYy-ZTNo3yxygM1TY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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" .
}