@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_head
{
this:
np:hasAssertion
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion
;
np:hasProvenance
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance
;
np:hasPublicationInfo
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion
a
np:Assertion
.
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance
a
np:Provenance
.
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion
{
miriam-gene:1789
a
ncit:C16612
.
lld:C1306459
a
ncit:C7057
.
dgn-gda:DGN36e6f1048924eb25416794d55fef4408
sio:SIO_000628
miriam-gene:1789
,
lld:C1306459
;
a
sio:SIO_001121
.
}
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_provenance
{
dgn-np:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_assertion
dcterms:description
"[Indeed, the de novo methyltransferase 3B (DNMT3B) has been recently found to be mutated in several types of cancer and in the immunodeficiency, centromeric region instability and facial anomalies syndrome (ICF), in which these mutations could be related to the loss of global DNA methylation.]. 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:23474979
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP358120.RArW0LiINA21jfEycYqSSydAV_mjU6GHz6_li_Rh-kWRc130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:06+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}