@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg
> .
@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:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_head
{
this:
np:hasAssertion
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_assertion
;
np:hasProvenance
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_provenance
;
np:hasPublicationInfo
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_assertion
a
np:Assertion
.
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_provenance
a
np:Provenance
.
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGNf32bf0b159aace6ddbfae53c357e0408
sio:SIO_000628
miriam-gene:2706
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_provenance
{
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_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 .
}
dgn-np:NP164527.RAJEDwUVqL2U42Upn61orCzjlp4azKh9evOfQ0px27WQg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}