@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_head
{
this:
np:hasAssertion
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_assertion
;
np:hasProvenance
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_provenance
;
np:hasPublicationInfo
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_assertion
a
np:Assertion
.
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_provenance
a
np:Provenance
.
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_assertion
{
miriam-gene:4205
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGNcdc0ef641832fb2dda5ce817c2cbbf64
sio:SIO_000628
miriam-gene:4205
,
lld:C1956346
;
a
sio:SIO_001121
.
}
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_provenance
{
dgn-np:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_assertion
dcterms:description
"[Recently, a mutation in the human MEF2A gene was reported to be responsible for an autosomal dominant form of coronary artery disease, so the purpose of the present study was to assess the significance of MEF2A mutations in Japanese subjects with myocardial infarction (MI).]. 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:16195615
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP515778.RA3JQCTZxY5M_2R0Y6dmu9jnepz7UMPnevuNZR9bGqblo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:38+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}