@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo
> .
@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:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_head
{
this:
np:hasAssertion
dgn-np:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_assertion
;
np:hasProvenance
dgn-np:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_provenance
;
np:hasPublicationInfo
dgn-np:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_assertion
a
np:Assertion
.
dgn-np:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_provenance
a
np:Provenance
.
dgn-np:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C0023449
a
ncit:C7057
.
dgn-gda:DGN9bea473ad73e08fd317a25c6c40e3fe1
sio:SIO_000628
miriam-gene:2187
,
lld:C0023449
;
a
sio:SIO_001121
.
}
dgn-np:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_provenance
{
dgn-np:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_assertion
dcterms:description
"[Mutations have also been found with lower frequency in other FAB subtype AML (6 cases), in myeloproliferative disorders (6 cases), in myelodysplastic syndrome (3 cases) and rarely in acute lymphoblastic leukemia (1 case).]. 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:12529654
;
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:NP225251.RA8BQ8c-rggnrVbAPa-LGTHdjVzkxZucNQaNS9OOOe3jo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}