@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA
> .
@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:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_head
{
this:
np:hasAssertion
dgn-np:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_assertion
;
np:hasProvenance
dgn-np:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_provenance
;
np:hasPublicationInfo
dgn-np:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_assertion
a
np:Assertion
.
dgn-np:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_provenance
a
np:Provenance
.
dgn-np:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_assertion
{
miriam-gene:3769
a
ncit:C16612
.
lld:C0344290
a
ncit:C7057
.
dgn-gda:DGN707534c76ad53518dc4c9f294c0b3dfc
sio:SIO_000628
miriam-gene:3769
,
lld:C0344290
;
a
sio:SIO_001121
.
}
dgn-np:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_provenance
{
dgn-np:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_assertion
dcterms:description
"[These results indicate that the KCNJ13 R162W mutation can cause SVD and further show that vitreoretinal degeneration can arise through mutations in genes whose products are not structural components of the vitreous.]. 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:18179896
;
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:NP270604.RAP2jDmcKD2DNMTom1VBm-mTIZfqkOTNOfKUiLd-68yjA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:31+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" .
}