@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ
> .
@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:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_head
{
this:
np:hasAssertion
dgn-np:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_assertion
;
np:hasProvenance
dgn-np:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_assertion
a
np:Assertion
.
dgn-np:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_provenance
a
np:Provenance
.
dgn-np:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_assertion
{
miriam-gene:10804
a
ncit:C16612
.
lld:C0018784
a
ncit:C7057
.
dgn-gda:DGN5779e3df7e376f28cdcb3df11b53e356
sio:SIO_000628
miriam-gene:10804
,
lld:C0018784
;
a
sio:SIO_001121
.
}
dgn-np:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_provenance
{
dgn-np:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_assertion
dcterms:description
"[These findings: (1) demonstrate that GJB2, GJB6 deletion and A1555G mutation account for a minor proportion of NSHHL in the Qatari population, (2) further strengthen the need to search for causative genes, (3) clearly contribute to establishing preventive strategies for NSHHL in Qatar and in the Gulf area.]. 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:22103400
;
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:NP403591.RAQfjQl8KoMepFxDRWA8STMq6p3cgsBl4Jbxo0Ag4FzzQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}