@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E
> .
@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:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_head
{
this:
np:hasAssertion
dgn-np:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_assertion
;
np:hasProvenance
dgn-np:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_provenance
;
np:hasPublicationInfo
dgn-np:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_assertion
a
np:Assertion
.
dgn-np:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_provenance
a
np:Provenance
.
dgn-np:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C0027831
a
ncit:C7057
.
dgn-gda:DGNda24706c459662797433ca2c87a3400f
sio:SIO_000628
miriam-gene:861
,
lld:C0027831
;
a
sio:SIO_001121
.
}
dgn-np:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_provenance
{
dgn-np:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_assertion
dcterms:description
"[These point towards a variety of candidate genes that could contribute to the pathogenesis of minimally differentiated acute myeloid leukemia, including the tumor suppressor genes TP53 and NF1, and reinforced the importance of RUNX1 in this leukemia.]. 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:19773259
;
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:NP447621.RAIY2S-HuP4fKT9r8_1fKwwemkLPoe9JPMji9Es4c2k3E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:27+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" .
}