@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA
> .
@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:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_head
{
this:
np:hasAssertion
dgn-np:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_assertion
;
np:hasProvenance
dgn-np:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_provenance
;
np:hasPublicationInfo
dgn-np:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_assertion
a
np:Assertion
.
dgn-np:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_provenance
a
np:Provenance
.
dgn-np:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_assertion
{
miriam-gene:3417
a
ncit:C16612
.
lld:C0376545
a
ncit:C7057
.
dgn-gda:DGNe06fb38316c8e49a19e873d4e904e3c1
sio:SIO_000628
miriam-gene:3417
,
lld:C0376545
;
a
sio:SIO_001121
.
}
dgn-np:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_provenance
{
dgn-np:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_assertion
dcterms:description
"[Somatic mutations in isocitrate dehydrogenase 1 and 2 (IDH1 and IDH2) were recently demonstrated in acute myeloid leukemia (AML), but their prevalence and prognostic impact remain to be explored in large extensively characterized AML series, and also in various other hematologic malignancies.]. 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:20538800
;
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:NP499148.RAKLgRLNRchZcL3F7iLxmh5IoV3ocs3tk8GXsODVg_KoA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:57+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" .
}