@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg
> .
@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:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_head
{
this:
np:hasAssertion
dgn-np:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_assertion
;
np:hasProvenance
dgn-np:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_provenance
;
np:hasPublicationInfo
dgn-np:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_assertion
a
np:Assertion
.
dgn-np:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_provenance
a
np:Provenance
.
dgn-np:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_assertion
{
miriam-gene:7709
a
ncit:C16612
.
lld:C0007193
a
ncit:C7057
.
dgn-gda:DGN0ec268df1d2e6d52c49c33f3e1bc2186
sio:SIO_000628
miriam-gene:7709
,
lld:C0007193
;
a
sio:SIO_001122
.
}
dgn-np:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_provenance
{
dgn-np:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_assertion
dcterms:description
"[This GWAS identified two loci involved in sporadic DCM, one of them probably implicates BAG3. Our results show that rare mutations in BAG3 contribute to monogenic forms of the disease, while common variant(s) in the same gene are implicated in sporadic DCM.]. 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:21459883
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP95956.RAofhwwzx-DLeDH10o_ixCqJoZcUEedK2E3GUXBYtISCg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:48+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" .
}