@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ
> .
@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:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_head
{
this:
np:hasAssertion
dgn-np:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_assertion
;
np:hasProvenance
dgn-np:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_assertion
a
np:Assertion
.
dgn-np:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_provenance
a
np:Provenance
.
dgn-np:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_assertion
{
miriam-gene:6277
a
ncit:C16612
.
lld:C0023890
a
ncit:C7057
.
dgn-gda:DGN25c1f6dd77db76459a08878ea605eb0a
sio:SIO_000628
miriam-gene:6277
,
lld:C0023890
;
a
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.
}
dgn-np:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_provenance
{
dgn-np:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_assertion
dcterms:description
"[Application of MboII PRA to samples from 241 Korean patients with chronic liver diseases of different clinical stages confirmed that F141L mutants were significantly related to HCC, even in comparison to liver cirrhosis (HCC, 26.3% of patients, or 26/99; liver cirrhosis, 3.8% of patients, or 2/52; P = 0.001).]. 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:20962085
;
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:NP465135.RAf2uDwHBpFxGDRzPZN1_qYnME3JEVU10mpZcHX-WvRUQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:39+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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dgn-void:disgenetrdf
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"v2.1.0" .
}