@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM
> .
@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:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_head
{
this:
np:hasAssertion
dgn-np:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_assertion
;
np:hasProvenance
dgn-np:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_provenance
;
np:hasPublicationInfo
dgn-np:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_assertion
a
np:Assertion
.
dgn-np:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_provenance
a
np:Provenance
.
dgn-np:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_assertion
{
miriam-gene:3418
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN459f815010698b71a36973ee12c82c4a
sio:SIO_000628
miriam-gene:3418
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_provenance
{
dgn-np:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_assertion
dcterms:description
"[This review surveys the prevalence of IDH mutations in cancer and explores current mechanistic understanding of IDH mutations with implications for diagnostic and therapeutic development for the treatment of gliomas and AML.]. 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:20692206
;
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:NP193451.RAmMr5zpTdXpIl3iiTrIDzWjtf6ehvO_78_TzEQzrqmdM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:46+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" .
}