@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4
> .
@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:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_head
{
this:
np:hasAssertion
dgn-np:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_assertion
;
np:hasProvenance
dgn-np:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_provenance
;
np:hasPublicationInfo
dgn-np:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_assertion
a
np:Assertion
.
dgn-np:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_provenance
a
np:Provenance
.
dgn-np:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_assertion
{
miriam-gene:920
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN32daab8a14cfdcc5204a7b484451a746
sio:SIO_000628
miriam-gene:920
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_provenance
{
dgn-np:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_assertion
dcterms:description
"[If the clinical utility of an absolute threshold for the diagnosis of CLL can be confirmed, it will be important to establish recommendations for standardization, similar to those employed for CD4 and CD34 enumeration.]. 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:23475845
;
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:NP473824.RAqjOWdEdAesw7AIDCDHSRH-LV2jDeQGpixRkGVb1Omt4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:44+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" .
}