@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY
> .
@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:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_head
{
this:
np:hasAssertion
dgn-np:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_assertion
;
np:hasProvenance
dgn-np:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_provenance
;
np:hasPublicationInfo
dgn-np:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_assertion
a
np:Assertion
.
dgn-np:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_provenance
a
np:Provenance
.
dgn-np:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_assertion
{
miriam-gene:7974
a
ncit:C16612
.
lld:C0023470
a
ncit:C7057
.
dgn-gda:DGN9131bd700bfe67166d723866a8a6f1aa
sio:SIO_000628
miriam-gene:7974
,
lld:C0023470
;
a
sio:SIO_001121
.
}
dgn-np:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_provenance
{
dgn-np:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_assertion
dcterms:description
"[Two of these partners, ENL and AF9, code for proteins that are highly similar to each other and as fusions with HRX induce myeloid leukemias in mice as demonstrated by retroviral gene transfer and knock-in experiments, respectively.]. 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:9418860
;
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:NP655896.RA4Y2W07xZ_4phaEu-B4A8WW18-x8LiwdtRce_nDV6bIY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:35+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" .
}