@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8
> .
@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:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_head
{
this:
np:hasAssertion
dgn-np:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_assertion
;
np:hasProvenance
dgn-np:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_provenance
;
np:hasPublicationInfo
dgn-np:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_assertion
a
np:Assertion
.
dgn-np:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_provenance
a
np:Provenance
.
dgn-np:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_assertion
{
miriam-gene:145226
a
ncit:C16612
.
lld:C1301509
a
ncit:C7057
.
dgn-gda:DGN8cbf11098bace44e5e64f2686b9290c3
sio:SIO_000628
miriam-gene:145226
,
lld:C1301509
;
a
sio:SIO_001121
.
}
dgn-np:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_provenance
{
dgn-np:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_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:NP329945.RAbKFpzirMzCFCC3ON4Bt2_15EX4kVoW_yn56l9kZMST8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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" .
}