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http://rdf.disgenet.org/nanopublications.trig#NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_provenance
a
np:Provenance
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dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_publicationInfo
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np:PublicationInfo
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{
miriam-gene:7422
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN9f13e2e0102eb2759bf01e3d973ab567
sio:SIO_000628
miriam-gene:7422
,
lld:C0242383
;
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.
}
dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_provenance
{
dgn-np:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_assertion
dcterms:description
"[The HTRA1-rs11200638 and CFH-rs1410996/-rs2274700 variants were associated with response to PDT in this study population. These variants may be used for genetic biomarkers to estimate visual outcomes and recurrences in the response to PDT with significant predictive power.]. 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:20678803
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59223.RAM2NEdfCVkHvTHFcXnE5ky7N7sY6RW7Rbe5W3e1ClWfw130_publicationInfo
{
this:
dcterms:created
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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
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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