@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM
> .
@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:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_head
{
this:
np:hasAssertion
dgn-np:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_assertion
;
np:hasProvenance
dgn-np:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_provenance
;
np:hasPublicationInfo
dgn-np:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_assertion
a
np:Assertion
.
dgn-np:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_provenance
a
np:Provenance
.
dgn-np:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_assertion
{
miriam-gene:1788
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN6d2302e6cf49223dc75df0b32d8486f4
sio:SIO_000628
miriam-gene:1788
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_provenance
{
dgn-np:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_assertion
dcterms:description
"[Here we describe the consequences of single amino acid mutations, including those implicated in the development of acute myeloid leukemia (AML) and myelodysplastic syndromes, at the DNMT3A·DNMT3A homotetramer and DNMT3A·DNMT3L heterotetramer interfaces.]. 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:21979949
;
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:NP925967.RAv-a7bxZ5q6M3ePhy5Kv42PjkM954H19NBsiUUiK93zM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}