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http://rdf.disgenet.org/nanopublications.trig#NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk
> .
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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#
> .
@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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
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dgn-np:NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_assertion
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np:hasProvenance
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a
np:Nanopublication
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dgn-np:NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_assertion
a
np:Assertion
.
dgn-np:NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_provenance
a
np:Provenance
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{
miriam-gene:1286
a
ncit:C16612
.
lld:C0022578
a
ncit:C7057
.
dgn-gda:DGNff15f79c9e3646e233c6c6fed7020ce2
sio:SIO_000628
miriam-gene:1286
,
lld:C0022578
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.
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dgn-np:NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_provenance
{
dgn-np:NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_assertion
dcterms:description
"[The absence of pathogenic mutations in VSX1, SOD1, COL4A3, and COL4A4 genes in our large number of unrelated keratoconus patients indicates that other genetic factors are involved in the development of this disorder; nevertheless, a significant correlation of a few polymorphisms indicates that there could be a link between specific polymorphisms and KC disease.]. 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:20664914
;
prov:wasDerivedFrom
dgn-void:befree-20140225
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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:NP398759.RAvBcFl9a9cJXrNYOZplQkaLByECWWNepy4Pl2SCUBhXk130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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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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> , <
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> ;
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