@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA
> .
@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:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_head
{
this:
np:hasAssertion
dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_assertion
;
np:hasProvenance
dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_provenance
;
np:hasPublicationInfo
dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_assertion
a
np:Assertion
.
dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_provenance
a
np:Provenance
.
dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_assertion
{
miriam-gene:924
a
ncit:C16612
.
lld:C0036920
a
ncit:C7057
.
dgn-gda:DGNa3e11e80df35462ddfb53d19eabd0a7d
sio:SIO_000628
miriam-gene:924
,
lld:C0036920
;
a
sio:SIO_001121
.
}
dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_provenance
{
dgn-np:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_assertion
dcterms:description
"[High-level expression of c-myb in the peripheral blood as assessed by quantitative RT-PCR constitutes an additional diagnostic parameter for SS and may be especially useful in cases in which morphological determination of Sézary cells or FACS analysis of CD7 and CD26 remain inconclusive.]. 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:16088151
;
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:NP696059.RAyn_fd_DBIRAaHE6kNMFzcDljtA4zg48c-52FbWCEocA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}