@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c
> .
@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:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_head
{
this:
np:hasAssertion
dgn-np:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_assertion
;
np:hasProvenance
dgn-np:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_provenance
;
np:hasPublicationInfo
dgn-np:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_assertion
a
np:Assertion
.
dgn-np:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_provenance
a
np:Provenance
.
dgn-np:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_assertion
{
miriam-gene:966
a
ncit:C16612
.
lld:C1536085
a
ncit:C7057
.
dgn-gda:DGN25c64443cb02033dccc1c39729534ba1
sio:SIO_000628
miriam-gene:966
,
lld:C1536085
;
a
sio:SIO_001121
.
}
dgn-np:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_provenance
{
dgn-np:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_assertion
dcterms:description
"[In maculae of AMD specimens, we found that the complement regulatory protein, CD59, was increased in regions of uninvolved retinal pigmented epithelium (RPE) of early AMD, but decreased in the RPE overlying drusen and in geographic atrophy, an advanced form of AMD.]. 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:23097248
;
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:NP557745.RAeDtC9kEzbJ3wkdO_G47njRNEFm_PzVQRSZbALp2q77c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}