@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk
> .
@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:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_head
{
this:
np:hasAssertion
dgn-np:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_assertion
;
np:hasProvenance
dgn-np:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_provenance
;
np:hasPublicationInfo
dgn-np:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_assertion
a
np:Assertion
.
dgn-np:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_provenance
a
np:Provenance
.
dgn-np:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_assertion
{
miriam-gene:5015
a
ncit:C16612
.
lld:C0154823
a
ncit:C7057
.
dgn-gda:DGN944a0ff53198be73092059e2850e6608
sio:SIO_000628
miriam-gene:5015
,
lld:C0154823
;
a
sio:SIO_001121
.
}
dgn-np:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_provenance
{
dgn-np:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_assertion
dcterms:description
"[The expression pattern of OTX2 in human embryos is consistent with the eye phenotypes observed in the patients, which range from bilateral anophthalmia to retinal defects resembling Leber congenital amaurosis and pigmentary retinopathy.]. 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:15846561
;
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:NP505254.RAvXm4MM5Z9UxsKi4OIjypyRBy0Ex6TmE9ILQqBLNfumk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:01+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" .
}