@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII
> .
@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:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_head
{
this:
np:hasAssertion
dgn-np:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_assertion
;
np:hasProvenance
dgn-np:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_provenance
;
np:hasPublicationInfo
dgn-np:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_assertion
a
np:Assertion
.
dgn-np:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_provenance
a
np:Provenance
.
dgn-np:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_assertion
{
miriam-gene:5959
a
ncit:C16612
.
lld:C1301509
a
ncit:C7057
.
dgn-gda:DGN306588f40df6197b1ab4956a7d6d5c2f
sio:SIO_000628
miriam-gene:5959
,
lld:C1301509
;
a
sio:SIO_001121
.
}
dgn-np:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_provenance
{
dgn-np:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_assertion
dcterms:description
"[The severe visual impairment of individuals with mutations in RDH12 is in marked contrast to the mild visual deficiency in individuals with fundus albipunctatus caused by mutations in RDH5, encoding another retinal dehydrogenase.]. 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:15258582
;
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:NP733452.RAe3NTV6G_kLsYgVDs3rilnh5eAw_JeJaSrXf5F5bFdII130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:25+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" .
}