@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU
> .
@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:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_head
{
this:
np:hasAssertion
dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_assertion
;
np:hasProvenance
dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_provenance
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np:hasPublicationInfo
dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_assertion
a
np:Assertion
.
dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_provenance
a
np:Provenance
.
dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0007194
a
ncit:C7057
.
dgn-gda:DGNf90569e478873277b28259d0b83d8318
sio:SIO_000628
miriam-gene:8170
,
lld:C0007194
;
a
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.
}
dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_provenance
{
dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_assertion
dcterms:description
"[In conclusion, our data suggest that 15 bp-deletion and C-insertion in the 5'UTR region of MEF2C could affect hypertrophic cardiomyopathy, potentially by affecting expression of MEF2C and therefore, the expression of their target cardiac proteins that are implicated in the hypertrophic process.]. 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:22718505
;
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 .
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dgn-np:NP185486.RABkqycfP3sU2TIHyUKUtPQU4Vaad4vTLm0jiGFQPs8mU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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
<
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> , <
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
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"v2.1.0" .
}