@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E
> .
@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:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_head
{
this:
np:hasAssertion
dgn-np:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_assertion
;
np:hasProvenance
dgn-np:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_provenance
;
np:hasPublicationInfo
dgn-np:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_assertion
a
np:Assertion
.
dgn-np:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_provenance
a
np:Provenance
.
dgn-np:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_assertion
{
miriam-gene:4297
a
ncit:C16612
.
lld:C0220615
a
ncit:C7057
.
dgn-gda:DGN7e34e81d9458da515b672be1007a8772
sio:SIO_000628
miriam-gene:4297
,
lld:C0220615
;
a
sio:SIO_001121
.
}
dgn-np:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_provenance
{
dgn-np:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_assertion
dcterms:description
"[Because the sensitivity of detecting MLL gene rearrangement by cytogenetic analysis is extremely low compared with Southern blotting analysis, the MLL gene may be involved in substantial numbers of adult AML cases, regardless of FAB subtype.]. 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:10846829
;
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:NP466027.RAdjrYeoCCnYN9rnBGe9xgC0iFKDdYw9o_XTwRyjn900E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:39+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" .
}