@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0
> .
@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:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_head
{
this:
np:hasAssertion
dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_assertion
;
np:hasProvenance
dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_provenance
;
np:hasPublicationInfo
dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_assertion
a
np:Assertion
.
dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_provenance
a
np:Provenance
.
dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_assertion
{
miriam-gene:8996
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGNceb95e9052bfcae3956a848ff8441780
sio:SIO_000628
miriam-gene:8996
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_provenance
{
dgn-np:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_assertion
dcterms:description
"[In 431 patients presenting with unexplained cytopenia(s) FCM results were compared to abnormal karyotyping and FISH results recognized as associated with myelodysplastic syndrome (MDS) in the 2008 WHO classification, to assess the degree of and types of phenotypic abnormalities observed using a previously reported flow cytometric scoring system (FCSS).]. 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:21520402
;
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:NP852926.RAHmsDy1-o6771OvjoOV6-TGM6jqtZCG2XolB9NsKBZ_0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:41+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" .
}