@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g
> .
@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:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_head
{
this:
np:hasAssertion
dgn-np:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_assertion
;
np:hasProvenance
dgn-np:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_provenance
;
np:hasPublicationInfo
dgn-np:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_assertion
a
np:Assertion
.
dgn-np:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_provenance
a
np:Provenance
.
dgn-np:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_assertion
{
miriam-gene:4901
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGN375aee82cbc604b6398738d977ca9efd
sio:SIO_000628
miriam-gene:4901
,
lld:C0035334
;
a
sio:SIO_001121
.
}
dgn-np:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_provenance
{
dgn-np:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_assertion
dcterms:description
"[To search for mutations in the neural retina leucine zipper (NRL) gene in patients with dominant retinitis pigmentosa and to compare the severity of disease in these patients with that observed previously in patients with dominant rhodopsin mutations.]. 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:11879142
;
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:NP726352.RAocwLaO-anaUIO7eIU-XzfrkkeWcqqLelkVqmYeZvz3g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:21+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" .
}