@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0
> .
@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:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_head
{
this:
np:hasAssertion
dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_assertion
;
np:hasProvenance
dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_provenance
;
np:hasPublicationInfo
dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_assertion
a
np:Assertion
.
dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_provenance
a
np:Provenance
.
dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_assertion
{
miriam-gene:23746
a
ncit:C16612
.
lld:C0521683
a
ncit:C7057
.
dgn-gda:DGN87a0df969445fd0e9d8bf2220f613a50
sio:SIO_000628
miriam-gene:23746
,
lld:C0521683
;
a
sio:SIO_001121
.
}
dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_provenance
{
dgn-np:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_assertion
dcterms:description
"[Drusenlike deposits were more selectively observed in patients with mutations in the AIPL1, CRB1, RPE65, and RPGRIP1 genes, whereas focal regions of peripheral chorioretinal atrophy were observed only in patients with AIPL1 or RPE65 variations.]. 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:16205573
;
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:NP255834.RA5DfNXkCYcWS7Bs9cQ6e6j9SI8aDBPYHxorKMiKI4cV0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}