@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs
> .
@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:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_head
{
this:
np:hasAssertion
dgn-np:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_assertion
;
np:hasProvenance
dgn-np:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_provenance
;
np:hasPublicationInfo
dgn-np:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_assertion
a
np:Assertion
.
dgn-np:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_provenance
a
np:Provenance
.
dgn-np:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_assertion
{
miriam-gene:4695
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN666029992e5f15659929e2efdfedee3e
sio:SIO_000628
miriam-gene:4695
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_provenance
{
dgn-np:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_assertion
dcterms:description
"[In 35 patients with normal karyotype and 16 patients with cytogenetic anomalies not presently associated with FAB subtypes the expected correlations of rather immature myeloid immunologic phenotypes with M1 and M2 morphology and CD14 expression in monoblastic leukemias was found.]. 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:1638477
;
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:NP283660.RAcI_unWmM6kVnJA9UDYY0OSf-D014dzX0MPLmkgPMejs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:40+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" .
}