@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns
> .
@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:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_head
{
this:
np:hasAssertion
dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_assertion
;
np:hasProvenance
dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_provenance
;
np:hasPublicationInfo
dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_assertion
a
np:Assertion
.
dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_provenance
a
np:Provenance
.
dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_assertion
{
miriam-gene:2125
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGNfed42c5a93b057d2947dfe2c556f1016
sio:SIO_000628
miriam-gene:2125
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_provenance
{
dgn-np:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_assertion
dcterms:description
"[The e1a2, b2a2 or b3a2 and c3a2 fusion mRNAs encode distinct fusion proteins (p190, p210 and p230, respectively), which are associated with different forms of leukemogenesis in humans and animal models.]. 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:10602422
;
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:NP263407.RAWYuhLs3L_GnpvSXPGNyhXizWL81KKwVAWTx6vxOugns130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}