@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s
> .
@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:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_head
{
this:
np:hasAssertion
dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_assertion
;
np:hasProvenance
dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_provenance
;
np:hasPublicationInfo
dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_assertion
a
np:Assertion
.
dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_provenance
a
np:Provenance
.
dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_assertion
{
miriam-gene:10804
a
ncit:C16612
.
lld:C0152268
a
ncit:C7057
.
dgn-gda:DGNec6ca0c559e5c1e3aa1b89ed42b1f69e
sio:SIO_000628
miriam-gene:10804
,
lld:C0152268
;
a
sio:SIO_001121
.
}
dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_provenance
{
dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_assertion
dcterms:description
"[Our recent studies indicate that nonsyndromic hearing loss (NSHL) in the Saudi Arabian population is genetically heterogeneous and is not caused by mutations in GJB2 and GJB6, the most common genes for deafness in various populations worldwide.]. 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:23510777
;
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 .
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dgn-np:NP284000.RAlNhyTiG7V0K8qQDAOZZFsNKPcrUXGIfjIaZNmIDNI5s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:40+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
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"v2.1.0" .
}