@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs
> .
@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:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_head
{
this:
np:hasAssertion
dgn-np:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_assertion
;
np:hasProvenance
dgn-np:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_provenance
;
np:hasPublicationInfo
dgn-np:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_assertion
a
np:Assertion
.
dgn-np:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_provenance
a
np:Provenance
.
dgn-np:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_assertion
{
miriam-gene:54790
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNdd58a5e0d99d7817988d05e7e66706e1
sio:SIO_000628
miriam-gene:54790
,
lld:C0023467
;
a
sio:SIO_001122
.
}
dgn-np:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_provenance
{
dgn-np:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_assertion
dcterms:description
"[We initially identified deletions or mutations in TET2 in three patients with myelodysplastic syndromes, in three of five patients with myeloproliferative disorders, in two patients with primary AML, and in one patient with secondary 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:19474426
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP94868.RA1e6WJ6PwlkEHmVzDXae2S2tUyf_eODNDytuuco1vFIs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:32+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" .
}