@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o
> .
@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:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_head
{
this:
np:hasAssertion
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_assertion
;
np:hasProvenance
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_provenance
;
np:hasPublicationInfo
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_assertion
a
np:Assertion
.
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_provenance
a
np:Provenance
.
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_assertion
{
miriam-gene:5914
a
ncit:C16612
.
lld:C0023487
a
ncit:C7057
.
dgn-gda:DGN2519780e21bd7b66b7cb2b0874c00c3e
sio:SIO_000628
miriam-gene:5914
,
lld:C0023487
;
a
sio:SIO_001121
.
}
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_provenance
{
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_assertion
dcterms:description
"[Epigenetic alterations have been described in several AMLs, and in some cases their origin has been studied in detail mechanistically (such as in acute promyelocytic leukemia, caused by the promyelocytic leukemia-retinoic acid receptor-α fusion protein).]. 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:25369368
;
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 .
}
dgn-np:NP1234898.RAqfWaKb7HLpzVs3DW20m8ghjIRr6T5PP15g3hqo56a9o130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:05+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}