@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw
> .
@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:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_head
{
this:
np:hasAssertion
dgn-np:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_assertion
;
np:hasProvenance
dgn-np:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_provenance
;
np:hasPublicationInfo
dgn-np:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_assertion
a
np:Assertion
.
dgn-np:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_provenance
a
np:Provenance
.
dgn-np:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0206669
a
ncit:C7057
.
dgn-gda:DGN373ed168a8ab8946b78d0dc5e06e29f2
sio:SIO_000628
miriam-gene:1029
,
lld:C0206669
;
a
sio:SIO_001121
.
}
dgn-np:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_provenance
{
dgn-np:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_assertion
dcterms:description
"[In conclusion, our results demonstrate that RASSF1A and p16(INK4a) inactivation by methylation are frequent events in hepatocellular carcinoma, but not in HCA, which is in contrast to HCC without cirrhosis, viral hepatitis, storage diseases, or genetic background.]. 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:12660822
;
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:NP488114.RAEsrz6pH1OThD9QroM1r5RPrT_i7ehvLPETCUfIY2Xcw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}