@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo
> .
@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:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_head
{
this:
np:hasAssertion
dgn-np:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_assertion
;
np:hasProvenance
dgn-np:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_provenance
;
np:hasPublicationInfo
dgn-np:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_assertion
a
np:Assertion
.
dgn-np:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_provenance
a
np:Provenance
.
dgn-np:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_assertion
{
miriam-gene:11186
a
ncit:C16612
.
lld:C0032927
a
ncit:C7057
.
dgn-gda:DGN2ec7bd1792c8dc9c2a0bf8f12a1ade74
sio:SIO_000628
miriam-gene:11186
,
lld:C0032927
;
a
sio:SIO_001121
.
}
dgn-np:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_provenance
{
dgn-np:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_assertion
dcterms:description
"[The detection of low concentrations in HBV carriers is consistent with previous findings that RASSF1A hypermethylation is an early event in HCC pathogenesis and can be found in premalignant liver tissues.]. 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:18653827
;
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:NP795390.RA_-oUPOg8vtvUblUoQxQJOe-5aeWbNAcKoD0haHpdUyo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}