@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU
> .
@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:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_head
{
this:
np:hasAssertion
dgn-np:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_assertion
;
np:hasProvenance
dgn-np:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance
;
np:hasPublicationInfo
dgn-np:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_assertion
a
np:Assertion
.
dgn-np:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance
a
np:Provenance
.
dgn-np:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_assertion
{
miriam-gene:860
a
ncit:C16612
.
lld:C0085669
a
ncit:C7057
.
dgn-gda:DGNbb33f90fb4e0098d0a8a2b16a45bbcdd
sio:SIO_000628
miriam-gene:860
,
lld:C0085669
;
a
sio:SIO_001121
.
}
dgn-np:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_provenance
{
dgn-np:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_assertion
dcterms:description
"[Mutations in the genes encoding the interacting proteins AML1 and CBFbeta are the most common genetic abnormalities in acute leukaemia, and congenital mutations in the related AML3 gene are associated with disorders of osteogenesis.]. 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:10856244
;
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:NP760522.RAgp5Ae18_rMiomvqVr4Oo5u5m_T8ww4wp0njDD42VUhU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}