@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_head
{
this:
np:hasAssertion
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_assertion
;
np:hasProvenance
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_assertion
a
np:Assertion
.
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_provenance
a
np:Provenance
.
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_assertion
{
miriam-gene:7306
a
ncit:C16612
.
lld:C0078918
a
ncit:C7057
.
dgn-gda:DGNf28e9291e48469dd75c674647c8dcc8c
sio:SIO_000628
miriam-gene:7306
,
lld:C0078918
;
a
sio:SIO_001121
.
}
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_provenance
{
dgn-np:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_assertion
dcterms:description
"[ROCA, which in southern African Blacks is caused by mutations in the TYRP1 gene, therefore should be referred to as OCA3, since this is the third locus that has been shown to cause an OCA phenotype in humans.]. 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:9345097
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1382692.RAmUAtaOWaYeGKWWVk0L8ZPQc3EdAvSkkFv2fUEuuoMAg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:12+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}