@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs
> .
@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:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_head
{
this:
np:hasAssertion
dgn-np:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_assertion
;
np:hasProvenance
dgn-np:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_provenance
;
np:hasPublicationInfo
dgn-np:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_assertion
a
np:Assertion
.
dgn-np:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_provenance
a
np:Provenance
.
dgn-np:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_assertion
{
miriam-gene:23746
a
ncit:C16612
.
lld:C0521683
a
ncit:C7057
.
dgn-gda:DGN139a325632e100e1b7cf59a19b04cae6
sio:SIO_000628
miriam-gene:23746
,
lld:C0521683
;
a
sio:SIO_001121
.
}
dgn-np:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_provenance
{
dgn-np:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_assertion
dcterms:description
"[Drusenlike deposits were more selectively observed in carriers with mutations in the AIPL1, CRB1, RPE65, and RPGRIP1 genes, whereas mild peripheral chorioretinal atrophy was only observed in AIPL1 and RPE65 carriers.]. 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:15691574
;
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:NP415529.RAHnMkK2PWrAwXAlJXD2sxSnRAj3xv3TYlrgavp1nWbzs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}