@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU
> .
@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:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_head
{
this:
np:hasAssertion
dgn-np:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_assertion
;
np:hasProvenance
dgn-np:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_provenance
;
np:hasPublicationInfo
dgn-np:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_assertion
a
np:Assertion
.
dgn-np:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_provenance
a
np:Provenance
.
dgn-np:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_assertion
{
miriam-gene:778
a
ncit:C16612
.
lld:C1848172
a
ncit:C7057
.
dgn-gda:DGN6e6cf5b63fe0a5fe79aa1e59d3a874a6
sio:SIO_000628
miriam-gene:778
,
lld:C1848172
;
a
sio:SIO_001121
.
}
dgn-np:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_provenance
{
dgn-np:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_assertion
dcterms:description
"[Our report of patient population mutation screening for both CSNBX genes, and our exclusion of RP2 and RGPR, indicates that mutations in CACNA1F and NYX are likely to account for all CSNBX.]. 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:12552565
;
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:NP352115.RACpUJr1ENtxTImM2qfkNNAbsVhBDOrENvsqneZS83bVU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}