@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k
> .
@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/v3.0.0/void/
> .
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_head
{
this:
np:hasAssertion
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_assertion
;
np:hasProvenance
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_provenance
;
np:hasPublicationInfo
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_assertion
a
np:Assertion
.
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_provenance
a
np:Provenance
.
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_assertion
{
miriam-gene:7531
a
ncit:C16612
.
lld:C0033027
a
ncit:C7057
.
dgn-gda:DGN399e3050abd121b46769fc0fd8b60f98
sio:SIO_000628
miriam-gene:7531
,
lld:C0033027
;
a
sio:SIO_001121
.
}
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_provenance
{
dgn-np:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_assertion
dcterms:description
"[Acquisition of the Philadelphia chromosome is an infrequent event in myelodysplastic syndrome, and the addition of this change to the initial genetic abnormality that caused MDS may have been associated with the accelerated clinical course of this patient.]. 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:12898186
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP781460.RAp57mHW5IkF0RP7UAb-S4T7sWaTUbH2UWu-4OprUFF6k130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:32+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}