@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_head
{
this:
np:hasAssertion
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_assertion
;
np:hasProvenance
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_provenance
;
np:hasPublicationInfo
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_assertion
a
np:Assertion
.
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_provenance
a
np:Provenance
.
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN90a50a4a23ec7a1158e256e9f54884e0
sio:SIO_000628
miriam-gene:861
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_provenance
{
dgn-np:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_assertion
dcterms:description
"[In contrast to AML-M0, the AML-M1 patient was trisomic for chromosome 21 and has two mutated and one normal RUNX1 allele, suggesting that the order of mutagenic events leading to leukemia may influence the predominant tumor type.]. 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:12555067
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP381919.RA_M_5u1x_j2x9V3MFgJFLel3cqx-KOOZQ5TIgUcvEPe8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:38+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}