@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4
> .
@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:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_head
{
this:
np:hasAssertion
dgn-np:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_assertion
;
np:hasProvenance
dgn-np:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_provenance
;
np:hasPublicationInfo
dgn-np:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_assertion
a
np:Assertion
.
dgn-np:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_provenance
a
np:Provenance
.
dgn-np:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_assertion
{
miriam-gene:4211
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNeadfedaee5c7e008343978d1e2cd875a
sio:SIO_000628
miriam-gene:4211
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_provenance
{
dgn-np:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_assertion
dcterms:description
"[Expression of HOX genes (A9, A10, B3 and B4), MEIS1 and MLL was easily detected in the majority of AML samples with the exception of two samples from patients with AML subtype M3 (which expressed only MLL).]. 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:10374871
;
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:NP687975.RAyH8HfJtw9QfCC-rVJw5teexNjpRwbTliXOBA0cPJux4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}