@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU
> .
@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:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_head
{
this:
np:hasAssertion
dgn-np:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_assertion
;
np:hasProvenance
dgn-np:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_provenance
;
np:hasPublicationInfo
dgn-np:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_assertion
a
np:Assertion
.
dgn-np:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_provenance
a
np:Provenance
.
dgn-np:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_assertion
{
miriam-gene:126393
a
ncit:C16612
.
lld:C0007193
a
ncit:C7057
.
dgn-gda:DGN48e944c9d99860da28935a3c8e77e99d
sio:SIO_000628
miriam-gene:126393
,
lld:C0007193
;
a
sio:SIO_001122
.
}
dgn-np:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_provenance
{
dgn-np:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_assertion
dcterms:description
"[To determine whether genetic variants exist in human Hsp20, which may modify these beneficial effects, we sequenced the coding region of the Hsp20 gene in 1347 patients suffering from dilated cardiomyopathy and 744 subjects with no heart disease.]. 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:18790732
;
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:NP76259.RA7zHfFKm6s-J5nrSvirJXO9p8fQVRrRAgnmw1cTcDQbU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:37+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" .
}