@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE
> .
@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:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_head
{
this:
np:hasAssertion
dgn-np:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_assertion
;
np:hasProvenance
dgn-np:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_provenance
;
np:hasPublicationInfo
dgn-np:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_assertion
a
np:Assertion
.
dgn-np:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_provenance
a
np:Provenance
.
dgn-np:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_assertion
{
miriam-gene:930
a
ncit:C16612
.
lld:C0019829
a
ncit:C7057
.
dgn-gda:DGNa3ea92a0b8f716638db76a14e1c6385a
sio:SIO_000628
miriam-gene:930
,
lld:C0019829
;
a
sio:SIO_001121
.
}
dgn-np:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_provenance
{
dgn-np:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_assertion
dcterms:description
"[The prevalence of B-cell restricted genes (CD19, CD20, and CD79b) suggests that this uniform population may be the clonal initiating (malignant) cells of Hodgkin lymphoma, despite their not showing translation to their respective proteins by immunohistochemical analysis.]. 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:23405135
;
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:NP488637.RALoxag7K7KReGTHzRBTFoWUMBJ2bAxy2u7BGeOL3wQBE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}