@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ
> .
@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:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_head
{
this:
np:hasAssertion
dgn-np:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_assertion
;
np:hasProvenance
dgn-np:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_assertion
a
np:Assertion
.
dgn-np:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_provenance
a
np:Provenance
.
dgn-np:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_assertion
{
miriam-gene:6648
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN8fb60ba1c57d86d2f1a1215f291ed7d1
sio:SIO_000628
miriam-gene:6648
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_provenance
{
dgn-np:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_assertion
dcterms:description
"[Taken together, these results indicate that epigenetic silencing of SOD2 could be facilitated by changes in histone modifications and represent one mechanism leading to the altered expression of MnSOD observed in many breast cancers.]. 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:18845242
;
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:NP510147.RAO1rhkSHYU55LkpIdyK7jl4pPhFV7YSfGy54zvS3ilcQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}