@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4
> .
@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:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_head
{
this:
np:hasAssertion
dgn-np:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_assertion
;
np:hasProvenance
dgn-np:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_provenance
;
np:hasPublicationInfo
dgn-np:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_assertion
a
np:Assertion
.
dgn-np:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_provenance
a
np:Provenance
.
dgn-np:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_assertion
{
miriam-gene:4869
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN818b69d79ea329e0a99561c0883da701
sio:SIO_000628
miriam-gene:4869
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_provenance
{
dgn-np:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_assertion
dcterms:description
"[Mutations in nucleophosmin (NPM) exon 12 and the resulting delocalization of NPM into the cytoplasm are the most specific and frequent cellular events in acute myeloid leukemia patients (AML) with normal karyotype.]. 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:18401421
;
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:NP665055.RA4BJPPKKTuSvGzL2wAeYOFriMKQdkMHKBCSpbVv24Ls4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:47+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" .
}