@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_head
{
this:
np:hasAssertion
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_assertion
;
np:hasProvenance
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_provenance
;
np:hasPublicationInfo
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_assertion
a
np:Assertion
.
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_provenance
a
np:Provenance
.
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_assertion
{
miriam-gene:25794
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGNc4042f021c033c3d648f11d48d183b9b
sio:SIO_000628
miriam-gene:25794
,
lld:C0035334
;
a
sio:SIO_001122
.
}
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_provenance
{
dgn-np:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_assertion
dcterms:description
"[ The Pro 23 His and Pro 347 Leu mutations in the rhodopsin gene are representative mutations for ADRP in other countries, but the mutation in the rhodopsin gene is very rare in Japanese patients with ADRP. On the other hand, a novel 208 delG mutation in t]. 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:14661542
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP52000.RAaw5NO4qNreTLkbI9bGjTroobhbgHntiDpzQO8ysMslY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:08+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}