@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU
> .
@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:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_head
{
this:
np:hasAssertion
dgn-np:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_assertion
;
np:hasProvenance
dgn-np:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_provenance
;
np:hasPublicationInfo
dgn-np:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_assertion
a
np:Assertion
.
dgn-np:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_provenance
a
np:Provenance
.
dgn-np:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_assertion
{
miriam-gene:2697
a
ncit:C16612
.
lld:C0011053
a
ncit:C7057
.
dgn-gda:DGN9d35312b181da623ba9473461f8c2d6f
sio:SIO_000628
miriam-gene:2697
,
lld:C0011053
;
a
sio:SIO_001121
.
}
dgn-np:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_provenance
{
dgn-np:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_assertion
dcterms:description
"[The results of this study suggest that the three mutations in GJA1 or rhoGJA1 that we previously reported result in at least partial loss of normal functions carried out by CX43, which may form a basis for the mechanism contributing to hearing loss in patients.]. 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:20130915
;
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:NP583851.RAno_fx2HYZFtPUfmhYUiIt9kNAEn7OSEfctzAHk1HGjU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}