@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU
> .
@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:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_head
{
this:
np:hasAssertion
dgn-np:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_assertion
;
np:hasProvenance
dgn-np:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_provenance
;
np:hasPublicationInfo
dgn-np:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_assertion
a
np:Assertion
.
dgn-np:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_provenance
a
np:Provenance
.
dgn-np:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_assertion
{
miriam-gene:4607
a
ncit:C16612
.
lld:C1449563
a
ncit:C7057
.
dgn-gda:DGN9af4c3a2dc4afc917de746e5d544875e
sio:SIO_000628
miriam-gene:4607
,
lld:C1449563
;
a
sio:SIO_001121
.
}
dgn-np:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_provenance
{
dgn-np:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_assertion
dcterms:description
"[Although cases of adult patients with DCM caused by mutations of the genes encoding sarcomeric or cytoskeletal proteins of cardiomyocytes are infrequent in Japan, it may be advisable to screen older DCM patients for MYBPC3 mutations, and male patients with familial DCM for dystrophin mutations.]. 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:15671604
;
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:NP720934.RAQj1raCwPjnRc4jckz66iUD41Z73Y5RUqv_gSf4h48yU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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" .
}