@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0
> .
@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/v4.0.0/void/
> .
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_head
{
this:
np:hasAssertion
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_assertion
;
np:hasProvenance
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_assertion
a
np:Assertion
.
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_provenance
a
np:Provenance
.
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_assertion
{
miriam-gene:4940
a
ncit:C16612
.
lld:C0030232
a
ncit:C7057
.
dgn-gda:DGN264d9cf24b873051d4784349831cf5e8
sio:SIO_000628
miriam-gene:4940
,
lld:C0030232
;
a
sio:SIO_001121
.
}
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_provenance
{
dgn-np:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_assertion
dcterms:description
"[In Leber hereditary optic neuropathy, a reduced N95 component of PERG and severely reduced VEP P100 may be present already in the acute stage of disease, before optic disc pallor appears, suggesting primary dysfunction of retinal ganglion cells.]. 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:25690485
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1264442.RAPIMFPmeZYsG1XoHso1LOQIxOM9saZL9VrJSpAHn-5h0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:19+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}