@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s130_assertion
a
np:Assertion
.
dgn-np:NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s130_provenance
a
np:Provenance
.
dgn-np:NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s130_publicationInfo
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.
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dgn-np:NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s130_assertion
{
miriam-gene:1796
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGNe9b2ed66be04a64376a3e006d1c6094b
sio:SIO_000628
miriam-gene:1796
,
lld:C2239176
;
a
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.
}
dgn-np:NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s130_provenance
{
dgn-np:NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s130_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
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sio:SIO_000772
miriam-pubmed:21146512
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP358314.RAF2RfFCZ_SOMa14XM3jjN7t9btSQNHCLL_k_6cueG90s130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:06+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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
"v3.0.0.0" .
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pav:version
"v3.0.0" .
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