@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I
> .
@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:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_head
{
this:
np:hasAssertion
dgn-np:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_assertion
;
np:hasProvenance
dgn-np:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_provenance
;
np:hasPublicationInfo
dgn-np:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_assertion
a
np:Assertion
.
dgn-np:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_provenance
a
np:Provenance
.
dgn-np:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_assertion
{
miriam-gene:7299
a
ncit:C16612
.
lld:C0268503
a
ncit:C7057
.
dgn-gda:DGN0e46303e00a78fa03d30cc15cc66da62
sio:SIO_000628
miriam-gene:7299
,
lld:C0268503
;
a
sio:SIO_001121
.
}
dgn-np:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_provenance
{
dgn-np:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_assertion
dcterms:description
"[(1978) to also obtain a genetical classification, supported by the hairbulb test, has not proved to be useful for the classification of tyrosinase negative (TNOCA), tyrosinase positive oculocutaneous albinism (TPOCA), and autosomal recessive ocular albinism (AROA) as genetically distinct forms.]. 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:3109790
;
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:NP361338.RAYuGmiZOwFSJZkYZHb6Y0Whpd53pngPeuf1On_aQhk4I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:31+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" .
}