@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso
> .
@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:NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso130_head
{
this:
np:hasAssertion
dgn-np:NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso130_assertion
;
np:hasProvenance
dgn-np:NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso130_provenance
;
np:hasPublicationInfo
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;
a
np:Nanopublication
.
dgn-np:NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso130_assertion
a
np:Assertion
.
dgn-np:NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso130_provenance
a
np:Provenance
.
dgn-np:NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:51268
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN73528b818c05cb2218102f6fbcf64dc7
sio:SIO_000628
miriam-gene:51268
,
lld:C0678222
;
a
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.
}
dgn-np:NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso130_provenance
{
dgn-np:NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso130_assertion
dcterms:description
"[In this study, we propose IPSO algorithm to improve the reliability of PSO for the identification of the best protective SNP barcodes (SNP combinations and genotypes with maximum difference between cases and controls) associated with breast 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:22623973
;
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:NP481343.RAZsX-pFNfT-vVv4tGUrOvqDjEEQw6AVj3g5PvYn7qlso130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}