@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk
> .
@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:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_head
{
this:
np:hasAssertion
dgn-np:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_assertion
;
np:hasProvenance
dgn-np:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_provenance
;
np:hasPublicationInfo
dgn-np:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_assertion
a
np:Assertion
.
dgn-np:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_provenance
a
np:Provenance
.
dgn-np:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_assertion
{
miriam-gene:79600
a
ncit:C16612
.
lld:C0431399
a
ncit:C7057
.
dgn-gda:DGN75abbe6f11471c7054d71334d3207f85
sio:SIO_000628
miriam-gene:79600
,
lld:C0431399
;
a
sio:SIO_001121
.
}
dgn-np:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_provenance
{
dgn-np:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_assertion
dcterms:description
"[Our study, the largest comprehensive molecular series on JS, provides independent confirmation of the recently reported TCTN1, TMEM237, and C5ORF42 as bona fide JS disease genes, and expands the allelic heterogeneity of this disease.]. 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:22693042
;
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:NP665193.RAeUlD2vEcsLall8ghk42TyKx82WjBmYG-igeZwWGvUxk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}