@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik
> .
@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:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_head
{
this:
np:hasAssertion
dgn-np:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_assertion
;
np:hasProvenance
dgn-np:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_provenance
;
np:hasPublicationInfo
dgn-np:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_assertion
a
np:Assertion
.
dgn-np:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_provenance
a
np:Provenance
.
dgn-np:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_assertion
{
miriam-gene:7127
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN3440772711085d6e8c4d9237a3c8ef02
sio:SIO_000628
miriam-gene:7127
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_provenance
{
dgn-np:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_assertion
dcterms:description
"[A screen of bone marrow cells from normal donors or patients with acute myelogenous leukemia showed that B94 was highly expressed in normal marrow and in marrow from patients with acute myelogenous leukemia French-American-British subtypes M0-M2, but was repressed in marrow cells from APL patients.]. 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:10766166
;
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:NP491162.RAvRB9Z1GedtktwA_HvPBwhyoUQXN0nehSa8jgeKwL5ik130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}