@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U
> .
@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:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_head
{
this:
np:hasAssertion
dgn-np:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_assertion
;
np:hasProvenance
dgn-np:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_provenance
;
np:hasPublicationInfo
dgn-np:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_assertion
a
np:Assertion
.
dgn-np:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_provenance
a
np:Provenance
.
dgn-np:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_assertion
{
miriam-gene:9541
a
ncit:C16612
.
lld:C0220615
a
ncit:C7057
.
dgn-gda:DGN44d7e16fcdaa06c182c157bf5bee4838
sio:SIO_000628
miriam-gene:9541
,
lld:C0220615
;
a
sio:SIO_001121
.
}
dgn-np:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_provenance
{
dgn-np:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_assertion
dcterms:description
"[We conclude that although the prognostic impact of many recurring abnormalities has not been ascertained independently of complex karyotype, cytogenetics is among the most useful factors predicting attainment of CR, CIR, and long-term survival in adult AML.]. 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:12393746
;
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:NP288132.RADKc6PE7Egwr7-YzUypARuvZu9K5UXWOXg7W3b2hup2U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:44+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" .
}