@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig
> .
@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:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_head
{
this:
np:hasAssertion
dgn-np:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_assertion
;
np:hasProvenance
dgn-np:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_provenance
;
np:hasPublicationInfo
dgn-np:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_assertion
a
np:Assertion
.
dgn-np:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_provenance
a
np:Provenance
.
dgn-np:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_assertion
{
miriam-gene:4291
a
ncit:C16612
.
lld:C0280028
a
ncit:C7057
.
dgn-gda:DGNec855095fa80e9def8002da6d1ce27f2
sio:SIO_000628
miriam-gene:4291
,
lld:C0280028
;
a
sio:SIO_001121
.
}
dgn-np:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_provenance
{
dgn-np:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_assertion
dcterms:description
"[According to the FAB classification, high levels of MLF1 were found in patients with relatively immature subtypes of AML (M1, M2, M6 and M7) and high risk MDS (RAEB and RAEB-T).]. 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:11021751
;
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:NP230914.RAqpZ_WAXH3PGVr99bP9e1IIx9C_Y61-qUUnGW86lltig130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:09+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" .
}