@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242612.RAuVcf4SQ6Llb91hELix7lGPIhja333X-ehBD_NOs7QRI
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP242612.RAuVcf4SQ6Llb91hELix7lGPIhja333X-ehBD_NOs7QRI130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP242612.RAuVcf4SQ6Llb91hELix7lGPIhja333X-ehBD_NOs7QRI130_assertion
a
np:Assertion
.
dgn-np:NP242612.RAuVcf4SQ6Llb91hELix7lGPIhja333X-ehBD_NOs7QRI130_provenance
a
np:Provenance
.
dgn-np:NP242612.RAuVcf4SQ6Llb91hELix7lGPIhja333X-ehBD_NOs7QRI130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:7157
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGNc1ff8368eab908da04914214a26877e7
sio:SIO_000628
miriam-gene:7157
,
lld:C0026986
;
a
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.
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dgn-np:NP242612.RAuVcf4SQ6Llb91hELix7lGPIhja333X-ehBD_NOs7QRI130_provenance
{
dgn-np:NP242612.RAuVcf4SQ6Llb91hELix7lGPIhja333X-ehBD_NOs7QRI130_assertion
dcterms:description
"[We applied the International Prognostic Scoring System (IPSS) to our series of 118 patients with myelodysplastic syndrome (MDS) to determine its validity, and also used univariate and multivariate analyses to evaluate the prognostic significance of TP53 configurations.]. 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:11703325
;
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 .
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dgn-np:NP242612.RAuVcf4SQ6Llb91hELix7lGPIhja333X-ehBD_NOs7QRI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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
> , <
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> , <
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
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"v2.1.0" .
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