@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU
> .
@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/v3.0.0/void/
> .
dgn-np:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_head
{
this:
np:hasAssertion
dgn-np:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_assertion
a
np:Assertion
.
dgn-np:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance
a
np:Provenance
.
dgn-np:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_assertion
{
miriam-gene:10982
a
ncit:C16612
.
lld:C0339525
a
ncit:C7057
.
dgn-gda:DGN8a95c7e3bf7c6d822c5cae330c100b04
sio:SIO_000628
miriam-gene:10982
,
lld:C0339525
;
a
sio:SIO_001121
.
}
dgn-np:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_provenance
{
dgn-np:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_assertion
dcterms:description
"[To examine the role of RP1 mutations in RP, we screened 101 unrelated Chinese RP patients (unselected for mode of inheritance) and 190 elderly normal control subjects for sequence changes in the coding exons for the 2156 amino acid RP1 protein.]. 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:11317367
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP857466.RATkygLqTd2wLEquMleEpMgzot292AXdt91iH4agi52aU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:20+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
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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
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v3.0.0.0" .
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"v3.0.0" .
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