@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ
> .
@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:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_head
{
this:
np:hasAssertion
dgn-np:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_assertion
;
np:hasProvenance
dgn-np:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_assertion
a
np:Assertion
.
dgn-np:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_provenance
a
np:Provenance
.
dgn-np:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_assertion
{
miriam-gene:4066
a
ncit:C16612
.
lld:C3463824
a
ncit:C7057
.
dgn-gda:DGNf7ff8248fc5317824c723f29d8d89afd
sio:SIO_000628
miriam-gene:4066
,
lld:C3463824
;
a
sio:SIO_001121
.
}
dgn-np:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_provenance
{
dgn-np:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_assertion
dcterms:description
"[Using real-time quantitative RT-PCR assay, we found that the expression of LYL1 was at higher levels in the majority cases of acute myeloblastic leukemia (AML) or myelodysplastic syndrome when compared to normal bone marrow.]. 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:16094422
;
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:NP228093.RASHhB-WEZMe7gzVuszWyaaezDRF2ij4RbP-zByQWmxQQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}