@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U
> .
@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:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_head
{
this:
np:hasAssertion
dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion
;
np:hasProvenance
dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance
;
np:hasPublicationInfo
dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion
a
np:Assertion
.
dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance
a
np:Provenance
.
dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion
{
miriam-gene:9968
a
ncit:C16612
.
lld:C0338508
a
ncit:C7057
.
dgn-gda:DGNdcacda6641b9fb1d484371d9c9e6e2a3
sio:SIO_000628
miriam-gene:9968
,
lld:C0338508
;
a
sio:SIO_001121
.
}
dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_provenance
{
dgn-np:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_assertion
dcterms:description
"[OPA1, the gene responsible for autosomal dominant optic atrophy represents an excellent candidate gene for NTG, as the clinical phenotypes are similar and OPA1 is expressed in the retina and optic nerve.]. 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:11810296
;
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:NP343261.RALa-c2d3mLDX96e4a_onCr2UdFgJ8JkO1R5S2eVprq3U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:21+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" .
}