@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU
> .
@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:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_head
{
this:
np:hasAssertion
dgn-np:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_assertion
;
np:hasProvenance
dgn-np:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_provenance
;
np:hasPublicationInfo
dgn-np:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_assertion
a
np:Assertion
.
dgn-np:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_provenance
a
np:Provenance
.
dgn-np:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_assertion
{
miriam-gene:865
a
ncit:C16612
.
lld:C1636667
a
ncit:C7057
.
dgn-gda:DGNb35e522bfaf00f2f04e6ac5d64c23f87
sio:SIO_000628
miriam-gene:865
,
lld:C1636667
;
a
sio:SIO_001121
.
}
dgn-np:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_provenance
{
dgn-np:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_assertion
dcterms:description
"[Acute myelomonocytic leukemia with eosinophilia is commonly associated with pericentric inversions of chromosome 16, involving the core binding factor beta gene (CBFB) on 16q22 and the myosin heavy chain gene (MYH11) on 16p13.]. 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:21763633
;
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:NP281554.RAca2KO0yXMeyV2qFlY1JCvMjoxUVltJaJAaBE5wXp-TU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}