@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ
> .
@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:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_head
{
this:
np:hasAssertion
dgn-np:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_assertion
;
np:hasProvenance
dgn-np:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_assertion
a
np:Assertion
.
dgn-np:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_provenance
a
np:Provenance
.
dgn-np:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_assertion
{
miriam-gene:6010
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGN165d84d34603190d166877956980c451
sio:SIO_000628
miriam-gene:6010
,
lld:C0035334
;
a
sio:SIO_001122
.
}
dgn-np:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_provenance
{
dgn-np:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_assertion
dcterms:description
"[Patients with RHO (D190N) autosomal dominant retinitis pigmentosa (adRP) can show classic signs of retinitis pigmentosa on fundus examination and may be able to maintain good central visual acuity into adulthood.]. 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:19085385
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP122241.RA1-WXqBZL5HVaKN_H0yS0R2cHB1mly3tuGweyKakMaPQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:03+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" .
}