@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U
> .
@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:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_head
{
this:
np:hasAssertion
dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_assertion
;
np:hasProvenance
dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_provenance
;
np:hasPublicationInfo
dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_assertion
a
np:Assertion
.
dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_provenance
a
np:Provenance
.
dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_assertion
{
miriam-gene:861
a
ncit:C16612
.
lld:C0033027
a
ncit:C7057
.
dgn-gda:DGNff0836e6a2359c6128bed8b15fba8e8f
sio:SIO_000628
miriam-gene:861
,
lld:C0033027
;
a
sio:SIO_001121
.
}
dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_provenance
{
dgn-np:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_assertion
dcterms:description
"[Somatic mutation of the AML1/RUNX1(RUNX1) gene is seen in acute myeloid leukemia (AML) M0 subtype and in AML transformed from myelodysplastic syndrome, but the impact of this gene mutation on survival in AML patients remains unclear.]. 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:19808697
;
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:NP315606.RAt3Kk4YvAxYJRCKZxtHCwLg_k0rxEqyFhNK0xIFP0a3U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}