@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc
> .
@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#
> .
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_head
{
this:
np:hasAssertion
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_assertion
;
np:hasProvenance
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_provenance
;
np:hasPublicationInfo
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_assertion
a
np:Assertion
.
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_provenance
a
np:Provenance
.
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_assertion
{
miriam-gene:5914
a
ncit:C16612
.
lld:C0023470
a
ncit:C7057
.
dgn-gda:DGN89c4d5a181c658c5df5639de900a68e5
sio:SIO_000628
miriam-gene:5914
,
lld:C0023470
;
a
sio:SIO_001121
.
}
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_provenance
{
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_assertion
dcterms:description
"[Acute promyelocytic leukemia (APL) is a distinct and paradigmatic subtype of myeloid leukemia associated with reciprocal chromosomal translocations always involving the Retinoic Acid Receptor(alpha) (RARalpha) gene on chromosome 17 and variable partner genes (X genes) on different chromosomes.]. 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:11607822
;
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 .
}
dgn-np:NP376433.RAR-HFO5_dAy5Py2qtGpt1U80vDLByxGAXV-1xIdjjELc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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
> , <
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}