@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA
> .
@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:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_head
{
this:
np:hasAssertion
dgn-np:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_assertion
;
np:hasProvenance
dgn-np:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_provenance
;
np:hasPublicationInfo
dgn-np:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_assertion
a
np:Assertion
.
dgn-np:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_provenance
a
np:Provenance
.
dgn-np:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C0023453
a
ncit:C7057
.
dgn-gda:DGNeb2c53aa37ba8b6e7632d63948e108c8
sio:SIO_000628
miriam-gene:2187
,
lld:C0023453
;
a
sio:SIO_001121
.
}
dgn-np:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_provenance
{
dgn-np:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_assertion
dcterms:description
"[Although leukemia with this chromosomal abnormality has been classified as L2 acute lymphoblastic leukemia by the FAB classification, two of our cases appeared to be of myelomonocyte origin as demonstrated by cytochemical, immunologic, and electron microscopic studies and differentiation induction by 12-tetradecanoyl-phorbol-13-acetate and methylformamide.]. 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:6340755
;
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:NP428033.RAUfR1of61xg546h7GaIkqoKRa2w2n1j2HQ4EqWE_mWlA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:13+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" .
}