@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ
> .
@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:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_head
{
this:
np:hasAssertion
dgn-np:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_assertion
;
np:hasProvenance
dgn-np:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_assertion
a
np:Assertion
.
dgn-np:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_provenance
a
np:Provenance
.
dgn-np:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C0730295
a
ncit:C7057
.
dgn-gda:DGNd780ad49072e7adf88b7e352599ce942
sio:SIO_000628
miriam-gene:3075
,
lld:C0730295
;
a
sio:SIO_001121
.
}
dgn-np:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_provenance
{
dgn-np:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_assertion
dcterms:description
"[Our findings strongly suggest that monogenic inheritance of CFH variants can result in basal laminar drusen in young adults, and this can progress to maculopathy and severe vision loss later in life.]. 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:18252232
;
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:NP488230.RA0E4u1a7KGIPetiHx0aBg8v0vo7AuiD3WlGN3_zVCfRQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}