@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP977161.RA4O49S0UhPCdrLeX7Pf8QMjfNLkTXpMCz_XTTbh78zT8
> .
@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/v4.0.0/void/
> .
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{
this:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP977161.RA4O49S0UhPCdrLeX7Pf8QMjfNLkTXpMCz_XTTbh78zT8130_publicationInfo
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a
np:Nanopublication
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dgn-np:NP977161.RA4O49S0UhPCdrLeX7Pf8QMjfNLkTXpMCz_XTTbh78zT8130_assertion
a
np:Assertion
.
dgn-np:NP977161.RA4O49S0UhPCdrLeX7Pf8QMjfNLkTXpMCz_XTTbh78zT8130_provenance
a
np:Provenance
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{
miriam-gene:6886
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGN5ba3cb37de077314fa148a8a5ff8afd0
sio:SIO_000628
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,
lld:C0699885
;
a
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.
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dgn-np:NP977161.RA4O49S0UhPCdrLeX7Pf8QMjfNLkTXpMCz_XTTbh78zT8130_provenance
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dgn-np:NP977161.RA4O49S0UhPCdrLeX7Pf8QMjfNLkTXpMCz_XTTbh78zT8130_assertion
dcterms:description
"[Validation in an independent sample of 212 BC patients enabled the optimization of five methylation targets, including VAX1, KCNV1, TAL1, PPOX1, and CFTR, which was obtained in our previous study, for BC diagnosis with a sensitivity and specificity of 88.68% and 87.25%, respectively.]. 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:22529986
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP977161.RA4O49S0UhPCdrLeX7Pf8QMjfNLkTXpMCz_XTTbh78zT8130_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
;
prv:usedData
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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
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