@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4
> .
@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:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_head
{
this:
np:hasAssertion
dgn-np:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_assertion
;
np:hasProvenance
dgn-np:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_provenance
;
np:hasPublicationInfo
dgn-np:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_assertion
a
np:Assertion
.
dgn-np:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_provenance
a
np:Provenance
.
dgn-np:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_assertion
{
miriam-gene:862
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN2c25106a4542dd484281db921eaf2cbc
sio:SIO_000628
miriam-gene:862
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_provenance
{
dgn-np:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_assertion
dcterms:description
"[In this issue of Blood,Matsuura and colleagues provide evidence that loss of GMCSF signaling promotes leukemic progression in association with one of the most frequently observed cytogenetic abnormalities in AML, the t(8;21)(q22;q22) that generates the RUNX1-ETO fusion protein.]. 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:22461472
;
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:NP347767.RAkZDCxgeqtkF7p4vPCz8--8ryrPPjXoNtxnIpSfj22t4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:24+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" .
}