@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ
> .
@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:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_head
{
this:
np:hasAssertion
dgn-np:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_assertion
;
np:hasProvenance
dgn-np:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_assertion
a
np:Assertion
.
dgn-np:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_provenance
a
np:Provenance
.
dgn-np:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_assertion
{
miriam-gene:5362
a
ncit:C16612
.
lld:C0271093
a
ncit:C7057
.
dgn-gda:DGN1e4d8baa298bba93952852c7a2e46d0a
sio:SIO_000628
miriam-gene:5362
,
lld:C0271093
;
a
sio:SIO_001121
.
}
dgn-np:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_provenance
{
dgn-np:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_assertion
dcterms:description
"[This study was conducted to correlate foveolar thickness (FT) and total macular volume (TMV), measured by optical coherence tomography (OCT), with other clinical characteristics and with specific genetic variation in Hungarian patients with arSTGD.]. 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:16303926
;
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:NP846419.RA5MIE21kt3cMHnx2U7tA1oylg-Eq97B9dOgNhoRvvjWQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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" .
}