@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw
> .
@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:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_head
{
this:
np:hasAssertion
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_assertion
;
np:hasProvenance
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_provenance
;
np:hasPublicationInfo
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_assertion
a
np:Assertion
.
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_provenance
a
np:Provenance
.
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_assertion
{
miriam-gene:3757
a
ncit:C16612
.
lld:C0008525
a
ncit:C7057
.
dgn-gda:DGN2bf9304bfa4d5acf90b2561702d446d5
sio:SIO_000628
miriam-gene:3757
,
lld:C0008525
;
a
sio:SIO_001121
.
}
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_provenance
{
dgn-np:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_assertion
dcterms:description
"[The carriers of XLRP who had evidence of photoreceptor cell dysfunction (as determined by visual field loss and reduced ERG amplitudes) had increased levels of intraocular straylight, whereas the carriers of CHM, who showed fundus abnormalities alone, in the absence of demonstrable photoreceptor cell dysfunction, had normal or minimally elevated levels.]. 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:11772598
;
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:NP402838.RAs6JIs-aFCOBOrerZms7yBxiOAAeUPzPwxyHovm6Xbdw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}