@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc
> .
@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:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_head
{
this:
np:hasAssertion
dgn-np:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_assertion
;
np:hasProvenance
dgn-np:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_provenance
;
np:hasPublicationInfo
dgn-np:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_assertion
a
np:Assertion
.
dgn-np:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_provenance
a
np:Provenance
.
dgn-np:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0334276
a
ncit:C7057
.
dgn-gda:DGN26ef49d1a7835f1c2a9917f1bed21be8
sio:SIO_000628
miriam-gene:7157
,
lld:C0334276
;
a
sio:SIO_001121
.
}
dgn-np:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_provenance
{
dgn-np:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_assertion
dcterms:description
"[These results suggest that methylation-related silencing of SFN occurs in both normal lung tissues and adenocarcinoma in situ, and that demethylation of the SFN promoter participates in the aberrant expression of SFN in invasive adenocarcinoma cells, independently of p53 alteration.]. 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:22310466
;
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:NP587136.RADD8jZZn3qLgvAtALnETAj98-BQjqa4bfLZc1IMjrbKc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}