@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA
> .
@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:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_head
{
this:
np:hasAssertion
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_assertion
;
np:hasProvenance
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_provenance
;
np:hasPublicationInfo
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_assertion
a
np:Assertion
.
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_provenance
a
np:Provenance
.
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_assertion
{
miriam-gene:1050
a
ncit:C16612
.
lld:C2939461
a
ncit:C7057
.
dgn-gda:DGNc87e9df5c233f8a11a90a1ab8e84d5ff
sio:SIO_000628
miriam-gene:1050
,
lld:C2939461
;
a
sio:SIO_001121
.
}
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_provenance
{
dgn-np:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_assertion
dcterms:description
"[Subtyping of acute myeloid leukemia requires an integration of information from the patient's clinical history (such as any prior preleukemic myeloid neoplasm or cytotoxic potentially leukemogenic therapy), the leukemia morphology, cytogenetic findings, and the mutation status of particular genes (NPM1, FLT3, and CEBPA).]. 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:23590662
;
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:NP848000.RA01zK6y1VZnjLmgeLQj_Zl1CrySFaC7jqfCnkHZz86uA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:38+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" .
}