@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4
> .
@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:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_head
{
this:
np:hasAssertion
dgn-np:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_assertion
;
np:hasProvenance
dgn-np:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_provenance
;
np:hasPublicationInfo
dgn-np:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_assertion
a
np:Assertion
.
dgn-np:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_provenance
a
np:Provenance
.
dgn-np:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_assertion
{
miriam-gene:6120
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN48c573d70c1ebb767c7a93faf801cd41
sio:SIO_000628
miriam-gene:6120
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_provenance
{
dgn-np:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_assertion
dcterms:description
"[Molecular and cellular changes in the old RPE may underlie susceptibility to genetic mutations that are found in AMD patients and may be associated with the pathogenesis of AMD in the elderly.]. 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:19129916
;
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:NP208333.RAeDJ0hLZnRgA2pYMfnGsoXXUR5rR1gL4MjZcGvIEFlY4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}