@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4
> .
@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:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_head
{
this:
np:hasAssertion
dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_assertion
;
np:hasProvenance
dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_provenance
;
np:hasPublicationInfo
dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_assertion
a
np:Assertion
.
dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_provenance
a
np:Provenance
.
dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_assertion
{
miriam-gene:25861
a
ncit:C16612
.
lld:C0581883
a
ncit:C7057
.
dgn-gda:DGN241f590a2f12293a483c17bcc7689615
sio:SIO_000628
miriam-gene:25861
,
lld:C0581883
;
a
sio:SIO_001121
.
}
dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_provenance
{
dgn-np:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_assertion
dcterms:description
"[The whirler (wi) mouse mutant, characterised by deafness and circling behaviour, maps to the corresponding region on the murine chromosome 4, thus suggesting that DFNB31 and whirler may result from orthologous gene defects.]. 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:11973626
;
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:NP724487.RA5CdDUBIWDg_dUd8WH1pC76fiCz6UDwYV2azke6PhsB4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}