@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI
> .
@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:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_head
{
this:
np:hasAssertion
dgn-np:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_assertion
;
np:hasProvenance
dgn-np:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_provenance
;
np:hasPublicationInfo
dgn-np:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_assertion
a
np:Assertion
.
dgn-np:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_provenance
a
np:Provenance
.
dgn-np:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_assertion
{
miriam-gene:56649
a
ncit:C16612
.
lld:C3711374
a
ncit:C7057
.
dgn-gda:DGNa6c0474d78a4c2fec0f7524006b9529c
sio:SIO_000628
miriam-gene:56649
,
lld:C3711374
;
a
sio:SIO_001121
.
}
dgn-np:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_provenance
{
dgn-np:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_assertion
dcterms:description
"[Mutations in TMPRSS3 encoding a transmembrane serine protease were reported to be associated with two different autosomal recessive nonsyndromic hearing loss (arNSHL) phenotypes, DFNB8 and DFNB10, in terms of residual hearing that may mandate different rehabilitation.]. 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:24526180
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP923768.RAmn4giG9ooKN4IkmzLkUzZ4UmsTi5LDHOkRcUb220aQI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:04+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" .
}