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http://rdf.disgenet.org/resource/nanopub/NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank
> .
@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/
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_assertion
a
np:Assertion
.
dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_provenance
a
np:Provenance
.
dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_assertion
{
miriam-gene:7399
a
ncit:C16612
.
lld:C0271097
a
ncit:C7057
.
dgn-gda:DGNde1fcb243b7bd25239457f5d3e6cefe7
sio:SIO_000628
miriam-gene:7399
,
lld:C0271097
;
a
sio:SIO_001121
.
}
dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_provenance
{
dgn-np:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_assertion
dcterms:description
"[Our results indicate that mutations in the USH2A gene and the resulting phenotype are probably modulated by other variables, such as modifying genes, epigenetics or environmental factors which may be of importance for better understanding the etiology of Usher syndrome.]. 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:24160897
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1122511.RAPhiU3vn23__BiUkql5fEhgdoi_Xzywk61K2IcO4rank130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:15+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
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
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pav:version
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"v4.0.0" .
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