@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE
> .
@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:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_head
{
this:
np:hasAssertion
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_assertion
;
np:hasProvenance
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_provenance
;
np:hasPublicationInfo
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_assertion
a
np:Assertion
.
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_provenance
a
np:Provenance
.
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_assertion
{
miriam-gene:4901
a
ncit:C16612
.
lld:C0339526
a
ncit:C7057
.
dgn-gda:DGN84d6cbf4a95d7ec082f81a050df1447a
sio:SIO_000628
miriam-gene:4901
,
lld:C0339526
;
a
sio:SIO_001121
.
}
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_provenance
{
dgn-np:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_assertion
dcterms:description
"[Since a locus for autosomal recessive retinitis pigmentosa (arRP) has been linked to markers at 14q11 and since mutations in rhodopsin can lead to RP, we sequenced genomic PCR products of the NRL gene and of the rhodopsin-Nrl response element from a panel of patients representing independent families with inherited retinal degeneration.]. 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:9344665
;
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:NP724643.RAwg3GGZKt8mqpdUMVOtFbLV173Lnb9w_PWJOo9FsTbXE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}