@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E
> .
@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:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_head
{
this:
np:hasAssertion
dgn-np:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_assertion
;
np:hasProvenance
dgn-np:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_assertion
a
np:Assertion
.
dgn-np:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_provenance
a
np:Provenance
.
dgn-np:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_assertion
{
miriam-gene:7178
a
ncit:C16612
.
lld:C0035334
a
ncit:C7057
.
dgn-gda:DGNadd97662c6a438ad15d036f1ae239a1b
sio:SIO_000628
miriam-gene:7178
,
lld:C0035334
;
a
sio:SIO_001121
.
}
dgn-np:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_provenance
{
dgn-np:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_assertion
dcterms:description
"[Furthermore, chelation with EDTA stabilizes the structure of both wild-type rhodopsin and the most prevalent rhodopsin RP mutation, P(23)H. These interactions suggest that homeostatic regulation of trace metal concentrations in the rod outer segment of the retina may be important both physiologically and for an important cluster of RP 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:19206210
;
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:NP279232.RADbnJsjk8pKiShatqgAkp5M93QAznooO_CcS6_fp8-2E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}