@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_head
{
this:
np:hasAssertion
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_assertion
;
np:hasProvenance
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_provenance
;
np:hasPublicationInfo
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_assertion
a
np:Assertion
.
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_provenance
a
np:Provenance
.
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN707c45f7990385c1d9a0b00757206b6a
sio:SIO_000628
miriam-gene:2706
,
lld:C0011053
;
a
sio:SIO_001122
.
}
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_provenance
{
dgn-np:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_assertion
dcterms:description
"[GJB2 mutations are responsible not only for deafness but also for the occurrence of vestibular dysfunction. However, vestibular dysfunction tends to be unilateral and less severe in comparison with that of bilateral deafness.]. 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:20377502
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP51493.RAX4dBvOPoaq8e92Klz6R_1-QyxbJcLW1C7uPo_uvqxT8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:08+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}