@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po
> .
@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:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_head
{
this:
np:hasAssertion
dgn-np:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_assertion
;
np:hasProvenance
dgn-np:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_provenance
;
np:hasPublicationInfo
dgn-np:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_assertion
a
np:Assertion
.
dgn-np:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_provenance
a
np:Provenance
.
dgn-np:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_assertion
{
miriam-gene:203859
a
ncit:C16612
.
lld:C0026850
a
ncit:C7057
.
dgn-gda:DGNa6b0c79b4cab7208e1dda3e8b3e8f825
sio:SIO_000628
miriam-gene:203859
,
lld:C0026850
;
a
sio:SIO_001121
.
}
dgn-np:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_provenance
{
dgn-np:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_assertion
dcterms:description
"[As ANO5 has also been found to be mutated in two different forms of muscular dystrophy, the finding of this third mutation in GDD adds clues to the role of ANO5 in these disorders.]. 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:23047743
;
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:NP691630.RAqYhGiESUy9SipJsYKzPLxkTzb2xsfKbsfV6xYywr2Po130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:00+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" .
}