@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4
> .
@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:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_head
{
this:
np:hasAssertion
dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_assertion
;
np:hasProvenance
dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_provenance
;
np:hasPublicationInfo
dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_assertion
a
np:Assertion
.
dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_provenance
a
np:Provenance
.
dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_assertion
{
miriam-gene:79784
a
ncit:C16612
.
lld:C0848765
a
ncit:C7057
.
dgn-gda:DGNaf2dd9edab004af59411856fd547c3df
sio:SIO_000628
miriam-gene:79784
,
lld:C0848765
;
a
sio:SIO_001121
.
}
dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_provenance
{
dgn-np:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_assertion
dcterms:description
"[Within the refined DFNA4 interval the public databases list more than 50 genes, from which several appear to be promising DFNA4 candidates due to similarities with animal models and with other causative genes involved in hearing disability.]. 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:15042303
;
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:NP472779.RA4cEKNmYBj62SOcy8v2THGpm1t-uuIU_PJE072qL3gw4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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" .
}