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http://rdf.disgenet.org/nanopublications.trig#NP192165.RAYAlNTZYj8MK9j5AH3YyOSjzkgIVpGon51qofSCDD1ZE
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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http://linkedlifedata.com/resource/umls/id/
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP192165.RAYAlNTZYj8MK9j5AH3YyOSjzkgIVpGon51qofSCDD1ZE130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP192165.RAYAlNTZYj8MK9j5AH3YyOSjzkgIVpGon51qofSCDD1ZE130_assertion
a
np:Assertion
.
dgn-np:NP192165.RAYAlNTZYj8MK9j5AH3YyOSjzkgIVpGon51qofSCDD1ZE130_provenance
a
np:Provenance
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dgn-np:NP192165.RAYAlNTZYj8MK9j5AH3YyOSjzkgIVpGon51qofSCDD1ZE130_publicationInfo
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{
miriam-gene:1029
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN72d422772c2dd52b451716de3a45418b
sio:SIO_000628
miriam-gene:1029
,
lld:C2239176
;
a
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.
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dgn-np:NP192165.RAYAlNTZYj8MK9j5AH3YyOSjzkgIVpGon51qofSCDD1ZE130_provenance
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dgn-np:NP192165.RAYAlNTZYj8MK9j5AH3YyOSjzkgIVpGon51qofSCDD1ZE130_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
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sio:SIO_000772
miriam-pubmed:12660822
;
prov:wasDerivedFrom
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prov:wasGeneratedBy
eco:ECO_0000203
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dgn-void:befree-20140225
pav:importedOn
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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 .
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dgn-np:NP192165.RAYAlNTZYj8MK9j5AH3YyOSjzkgIVpGon51qofSCDD1ZE130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
dgn-void:disgenetrdf
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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