@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP505398.RAcMOEnRLm-JGrD1PE19QNOaT1WGDgLujeOMG0KFIVqgI
> .
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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/
> .
@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#
> .
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{
this:
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP505398.RAcMOEnRLm-JGrD1PE19QNOaT1WGDgLujeOMG0KFIVqgI130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP505398.RAcMOEnRLm-JGrD1PE19QNOaT1WGDgLujeOMG0KFIVqgI130_assertion
a
np:Assertion
.
dgn-np:NP505398.RAcMOEnRLm-JGrD1PE19QNOaT1WGDgLujeOMG0KFIVqgI130_provenance
a
np:Provenance
.
dgn-np:NP505398.RAcMOEnRLm-JGrD1PE19QNOaT1WGDgLujeOMG0KFIVqgI130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:55743
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNbc4d2c8a66ac384e7b8e26e9c241f22e
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miriam-gene:55743
,
lld:C0006826
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.
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{
dgn-np:NP505398.RAcMOEnRLm-JGrD1PE19QNOaT1WGDgLujeOMG0KFIVqgI130_assertion
dcterms:description
"[This is the first description of aberrant hypermethylation of the CHFR gene in any type of human cancer, and provides further evidence of the involvement of multiple checkpoint alterations in lung cancer.]. 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:11948416
;
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 .
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dgn-np:NP505398.RAcMOEnRLm-JGrD1PE19QNOaT1WGDgLujeOMG0KFIVqgI130_publicationInfo
{
this:
dcterms:created
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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
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prv:usedData
dgn-void:disgenetrdf
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> , <
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> ;
pav:createdBy
<
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