@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk
> .
@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:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_head
{
this:
np:hasAssertion
dgn-np:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_assertion
;
np:hasProvenance
dgn-np:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_provenance
;
np:hasPublicationInfo
dgn-np:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_assertion
a
np:Assertion
.
dgn-np:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_provenance
a
np:Provenance
.
dgn-np:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_assertion
{
miriam-gene:9381
a
ncit:C16612
.
lld:C0581883
a
ncit:C7057
.
dgn-gda:DGN945fa124ee1eb3229f2371a64d45bc71
sio:SIO_000628
miriam-gene:9381
,
lld:C0581883
;
a
sio:SIO_001121
.
}
dgn-np:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_provenance
{
dgn-np:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_assertion
dcterms:description
"[The polymorphic site may become useful for studying the origin of different OTOF mutations within various populations, for assessing recombination events within large pedigrees as well as founder effects and for association studies in further deafness phenotypes.]. 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:12469219
;
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:NP197572.RANs7P9ADUg-og1wxD49UUwOo3kmrBqwx88z0BgpeefEk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}