@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo130_head
{
this:
np:hasAssertion
dgn-np:NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo130_assertion
a
np:Assertion
.
dgn-np:NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo130_provenance
a
np:Provenance
.
dgn-np:NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:7531
a
ncit:C16612
.
lld:C3463824
a
ncit:C7057
.
dgn-gda:DGNf75968a6fb55ccbbdd629f64e1f8d99d
sio:SIO_000628
miriam-gene:7531
,
lld:C3463824
;
a
sio:SIO_001121
.
}
dgn-np:NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo130_provenance
{
dgn-np:NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo130_assertion
dcterms:description
"[We document an apparent role of FOXP1 and TP63, up to now poorly documented, in the progression of MDS in our patient who is lacking mutations in the TP53 tumor suppressor gene normally associated with poor outcome in myelodysplastic syndrome with 5q-.]. 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:24893616
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1188440.RAnstVSToyqY8UTk5uainDIye7Jv4T1VoAGNE8hF6olAo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:44+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
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;
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
"v4.0.0.0" .
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pav:version
"v4.0.0" .
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