@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404
> .
@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:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_head
{
this:
np:hasAssertion
dgn-np:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion
;
np:hasProvenance
dgn-np:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_provenance
;
np:hasPublicationInfo
dgn-np:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion
a
np:Assertion
.
dgn-np:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_provenance
a
np:Provenance
.
dgn-np:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion
{
miriam-gene:92211
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGN22e22a495d4ef4e62bf19c2ecef8bab3
sio:SIO_000628
miriam-gene:92211
,
lld:C0035334
;
a
sio:SIO_001122
.
}
dgn-np:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_provenance
{
dgn-np:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_assertion
dcterms:description
"[ PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined. Our data may facilitate future investigations of patients with various (other) forms of inherited retinal ]. 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:16288196
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP97176.RAQTmnuMzpcwLb20jFx8F1S6uL7I5p_NUp36b9pxjC404130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:32+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" .
}