@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g
> .
@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:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_head
{
this:
np:hasAssertion
dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_assertion
;
np:hasProvenance
dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_provenance
;
np:hasPublicationInfo
dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_assertion
a
np:Assertion
.
dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_provenance
a
np:Provenance
.
dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_assertion
{
miriam-gene:5456
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGNfa93c8c5062cd17b9ea4c8ae58de55df
sio:SIO_000628
miriam-gene:5456
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_provenance
{
dgn-np:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_assertion
dcterms:description
"[Since most of the mutations reported for DFN3 thus far are associated with regions that encode the DNA binding domains of POU3F4, our results strongly suggest that the deafness in DFN3 patients is largely due to the null function of POU3F4.]. 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:19671658
;
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:NP304642.RAVSdLVcYFQ2N4KyElKpEAnCjJpWGy9L27XGsAkOm7Z5g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}