@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU
> .
@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:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_head
{
this:
np:hasAssertion
dgn-np:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_assertion
;
np:hasProvenance
dgn-np:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_provenance
;
np:hasPublicationInfo
dgn-np:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_assertion
a
np:Assertion
.
dgn-np:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_provenance
a
np:Provenance
.
dgn-np:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_assertion
{
miriam-gene:420
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN6352bc194ad21af652cdbcaf6bc3fcc2
sio:SIO_000628
miriam-gene:420
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_provenance
{
dgn-np:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_assertion
dcterms:description
"[We found a high frequency of aberrant hypermethylation of specific genes (RASSF1A, GSTP1, CHRNA3, and DOK1) in HCC tumors as compared to control cirrhotic or normal liver tissues, suggesting that aberrant hypermethylation exhibits non-random and tumor-specific patterns in HCC.]. 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:21146512
;
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:NP568300.RAtWgwYVpKJAeYFr92b82qfy8GpBt1kkdSVbolF7YCBqU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:43+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" .
}