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http://rdf.disgenet.org/nanopublications.trig#NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_assertion
a
np:Assertion
.
dgn-np:NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance
a
np:Provenance
.
dgn-np:NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:3417
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGNa872399f0397c9aed0d6adde5621603a
sio:SIO_000628
miriam-gene:3417
,
lld:C0026986
;
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.
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dgn-np:NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_provenance
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dgn-np:NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_assertion
dcterms:description
"[We examined 193 patients with myelodysplastic syndromes and 53 patients with acute myeloid leukemia arising from myelodysplastic syndromes for mutations in IDH1 (R132), IDH2 (R172 and R140), and NPM1 by direct sequencing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:20494930
;
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 .
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dgn-np:NP201169.RA9LkxUEbt5rrq7mrJjFu-auHAivSGUT2zkE1ksWtfZSQ130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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