@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ
> .
@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:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_head
{
this:
np:hasAssertion
dgn-np:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_assertion
;
np:hasProvenance
dgn-np:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_assertion
a
np:Assertion
.
dgn-np:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_provenance
a
np:Provenance
.
dgn-np:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN1180ce9017b312a607d04c19d81102a1
sio:SIO_000628
miriam-gene:3918
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_provenance
{
dgn-np:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_assertion
dcterms:description
"[We believe that the evaluation of B-cell clonality in CSF requires multiple snPCR amplification on the same sample to compare the size of the products and, if necessary, the DNA sequences to ascertain the diagnosis of malignancy in equivocal cytologic and clinical findings.]. 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:9359512
;
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:NP434782.RAEju_S-T14fHDKcTvx7VpN5PfxC8Wa8IAHlsp5T4DxEQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:17+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" .
}