@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os
> .
@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:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_head
{
this:
np:hasAssertion
dgn-np:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_assertion
;
np:hasProvenance
dgn-np:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_provenance
;
np:hasPublicationInfo
dgn-np:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_assertion
a
np:Assertion
.
dgn-np:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_provenance
a
np:Provenance
.
dgn-np:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_assertion
{
miriam-gene:3757
a
ncit:C16612
.
lld:C0008525
a
ncit:C7057
.
dgn-gda:DGN3fde0940fda5e73aa585c02d18ddb238
sio:SIO_000628
miriam-gene:3757
,
lld:C0008525
;
a
sio:SIO_001121
.
}
dgn-np:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_provenance
{
dgn-np:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_assertion
dcterms:description
"[The abnormal BRB in XLRP carriers, with or without peripheral fundus pigmentary changes, was associated with at least moderate to moderately extensive reduction in scotopic ERG amplitudes, while the normal VF results in choroideremia carriers were associated with normal scotopic ERG amplitudes.]. 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:2916974
;
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:NP629203.RASA70VoroneIat6EkIsj4e-h5Hnd4-dFVJ3nSy40U8os130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:19+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: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" .
}