@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY
> .
@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:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_head
{
this:
np:hasAssertion
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_assertion
;
np:hasProvenance
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_provenance
;
np:hasPublicationInfo
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_assertion
a
np:Assertion
.
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_provenance
a
np:Provenance
.
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_assertion
{
miriam-gene:1756
a
ncit:C16612
.
lld:C0878544
a
ncit:C7057
.
dgn-gda:DGNbde657a37b24c1fc6b972cac9b83204c
sio:SIO_000628
miriam-gene:1756
,
lld:C0878544
;
a
sio:SIO_001122
.
}
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_provenance
{
dgn-np:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_assertion
dcterms:description
"[ Early diagnosis and treatment of DCM may lead to ventricular remodeling in DMD/BMD patients. Specific dystrophin gene mutations appear to be predictive of cardiac involvement, while other mutations may protect against or inhibit development of DCM. Further studies evaluating the impact of early intervention strategies on left ventricular geometry and function in muscular dystrophy patients seem warranted.]. 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:16246949
;
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:NP62760.RAx5fsXP98zwH6uImlu9hNFqTagG-lORqUl7otX-VPEvY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}