@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q
> .
@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:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_head
{
this:
np:hasAssertion
dgn-np:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_assertion
;
np:hasProvenance
dgn-np:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_assertion
a
np:Assertion
.
dgn-np:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_provenance
a
np:Provenance
.
dgn-np:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_assertion
{
miriam-gene:5015
a
ncit:C16612
.
lld:C0339527
a
ncit:C7057
.
dgn-gda:DGN6d7f57ac8f92ff8fa814f24f54061d45
sio:SIO_000628
miriam-gene:5015
,
lld:C0339527
;
a
sio:SIO_001121
.
}
dgn-np:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_provenance
{
dgn-np:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_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:NP929146.RAeNK6cNdMfHvSBSL1Mgqo3MgZk5zWhmOP92sLM7OKs_Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:30+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" .
}