@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA
> .
@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:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_head
{
this:
np:hasAssertion
dgn-np:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_assertion
;
np:hasProvenance
dgn-np:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_provenance
;
np:hasPublicationInfo
dgn-np:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_assertion
a
np:Assertion
.
dgn-np:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_provenance
a
np:Provenance
.
dgn-np:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_assertion
{
miriam-gene:8874
a
ncit:C16612
.
lld:C0339525
a
ncit:C7057
.
dgn-gda:DGN67510dedbac60eabcba4ec623f1f1b47
sio:SIO_000628
miriam-gene:8874
,
lld:C0339525
;
a
sio:SIO_001121
.
}
dgn-np:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_provenance
{
dgn-np:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_assertion
dcterms:description
"[Index patients from 15 independent families with adRP in which RHO mutations had been excluded in previous examinations were screened for mutations in the RP1 gene by means of direct DNA sequencing.]. 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:11864893
;
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:NP624642.RAxV2NSGAM6QahyntsIfdBmRfe4ImW-XVn1rUUQ1EMjfA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:17+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" .
}