@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo
> .
@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:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_head
{
this:
np:hasAssertion
dgn-np:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_assertion
;
np:hasProvenance
dgn-np:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_provenance
;
np:hasPublicationInfo
dgn-np:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_assertion
a
np:Assertion
.
dgn-np:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_provenance
a
np:Provenance
.
dgn-np:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_assertion
{
miriam-gene:4647
a
ncit:C16612
.
lld:C1832187
a
ncit:C7057
.
dgn-gda:DGN5ab021280e9d9e240326b3ef42b53894
sio:SIO_000628
miriam-gene:4647
,
lld:C1832187
;
a
sio:SIO_001121
.
}
dgn-np:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_provenance
{
dgn-np:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_assertion
dcterms:description
"[The critical regions for the recessive deafness locus DFNB2 and the dominant locus DFNA11, which were previously localized to the long arm of chromosome 11, do not overlap with the candidate interval of DFNA12.]. 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:9150164
;
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:NP633343.RALG2RTgk_ADOze5ygIAffUoj83vSPcPxWF2Zu5KrU0eo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:22+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" .
}