@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU
> .
@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:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_head
{
this:
np:hasAssertion
dgn-np:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_assertion
;
np:hasProvenance
dgn-np:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_provenance
;
np:hasPublicationInfo
dgn-np:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_assertion
a
np:Assertion
.
dgn-np:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_provenance
a
np:Provenance
.
dgn-np:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_assertion
{
miriam-gene:4942
a
ncit:C16612
.
lld:C0000744
a
ncit:C7057
.
dgn-gda:DGN035f20f59d2ee7ae275294d85a1f91a2
sio:SIO_000628
miriam-gene:4942
,
lld:C0000744
;
a
sio:SIO_001121
.
}
dgn-np:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_provenance
{
dgn-np:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_assertion
dcterms:description
"[In certain forms of retinitis pigmentosa, such as Refsum disease, gyrate atrophy of the choroid and retina, and abetalipoproteinemia, exact biochemical defects have been identified and specific treatments have been applied with some success.]. 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:10340561
;
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:NP752655.RATD1c2c71Gs23-pvnEEmy0SH_DyFn14rH0GNpcfIfUEU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:36+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" .
}