@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY
> .
@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:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_head
{
this:
np:hasAssertion
dgn-np:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_assertion
;
np:hasProvenance
dgn-np:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_provenance
;
np:hasPublicationInfo
dgn-np:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_assertion
a
np:Assertion
.
dgn-np:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_provenance
a
np:Provenance
.
dgn-np:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_assertion
{
miriam-gene:1211
a
ncit:C16612
.
lld:C0339527
a
ncit:C7057
.
dgn-gda:DGNb20c1a783ac79502267829ba8ab962ce
sio:SIO_000628
miriam-gene:1211
,
lld:C0339527
;
a
sio:SIO_001121
.
}
dgn-np:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_provenance
{
dgn-np:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_assertion
dcterms:description
"[The data obtained from this study will help clinicians provide counseling on visual prognosis to patients with known mutations in LCA genes and be of value in future studies aimed at the treatment of LCA and early childhood-onset RP.]. 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:20079931
;
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:NP407221.RA0VkdMtdxWVwMm79hi3xnVUoTXNo13G8dj_Y0hdStEHY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:02+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" .
}