@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec
> .
@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:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_head
{
this:
np:hasAssertion
dgn-np:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_assertion
;
np:hasProvenance
dgn-np:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_provenance
;
np:hasPublicationInfo
dgn-np:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_assertion
a
np:Assertion
.
dgn-np:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_provenance
a
np:Provenance
.
dgn-np:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_assertion
{
miriam-gene:10205
a
ncit:C16612
.
lld:C0266589
a
ncit:C7057
.
dgn-gda:DGN86748481ed8fbd50d61877f7848a8f3d
sio:SIO_000628
miriam-gene:10205
,
lld:C0266589
;
a
sio:SIO_001121
.
}
dgn-np:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_provenance
{
dgn-np:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_assertion
dcterms:description
"[Among them, 28 patients with isolated Mondini dysplasia (MD group), 50 patients with enlarged vestibular aqueduct with Mondini dysplasia (EVA with MD group), 50 patients with enlarged vestibular aqueduct without Mondini dysplasia (EVA group), and 16 patients with other types of inner ear malformations (IEM group) were identified.]. 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:21961810
;
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:NP696469.RAfTbwOmER6-ZSw65fdO8Oak71F6q4nsUiqcEQqP7r8ec130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}