@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE
> .
@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:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_head
{
this:
np:hasAssertion
dgn-np:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_assertion
;
np:hasProvenance
dgn-np:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_provenance
;
np:hasPublicationInfo
dgn-np:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_assertion
a
np:Assertion
.
dgn-np:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_provenance
a
np:Provenance
.
dgn-np:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_assertion
{
miriam-gene:2489
a
ncit:C16612
.
lld:C0154832
a
ncit:C7057
.
dgn-gda:DGNbb16c1cb1af95daaee8f04d3a4f2edd8
sio:SIO_000628
miriam-gene:2489
,
lld:C0154832
;
a
sio:SIO_001121
.
}
dgn-np:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_provenance
{
dgn-np:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_assertion
dcterms:description
"[We searched a North American FSHD registry and the University of Rochester (UR) FSHD research database, reviewed the literature, and sent surveys to 14 FSHD referral centers in the United States and overseas to identify patients with genetically confirmed FSHD1 with a diagnosis of Coats syndrome.]. 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:23446679
;
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:NP648457.RALwDoEaA4xefbFopkH8bCGYCZyula_2pacwQHrqm0rBE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}