@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w
> .
@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:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_head
{
this:
np:hasAssertion
dgn-np:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_assertion
;
np:hasProvenance
dgn-np:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_provenance
;
np:hasPublicationInfo
dgn-np:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_assertion
a
np:Assertion
.
dgn-np:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_provenance
a
np:Provenance
.
dgn-np:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C3463824
a
ncit:C7057
.
dgn-gda:DGNa15b15554d1a063913be339ef2f98dba
sio:SIO_000628
miriam-gene:861
,
lld:C3463824
;
a
sio:SIO_001121
.
}
dgn-np:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_provenance
{
dgn-np:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_assertion
dcterms:description
"[Observations for mutations of the Runt domain of the AML1 gene in bone marrow cells were made in 300 patients, including 131 with acute myeloid leukemia (AML), 94 with myelodysplastic syndrome (MDS), 28 with blast crisis chronic myeloid leukemia (CML), 3 with atypical CML, 41 with acute lymphoblastic leukemia (ALL), and 3 with essential thrombocythemia (ET).]. 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:11023523
;
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:NP288882.RAg8_IsD_jrpH8Tgv7FCT2aBapKy6--YcMYE_6sjjij4w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:44+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" .
}