@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94
> .
@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:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_head
{
this:
np:hasAssertion
dgn-np:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_assertion
;
np:hasProvenance
dgn-np:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_provenance
;
np:hasPublicationInfo
dgn-np:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_assertion
a
np:Assertion
.
dgn-np:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_provenance
a
np:Provenance
.
dgn-np:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_assertion
{
miriam-gene:4205
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGN8f554c197906f7bfc9168c3551da406c
sio:SIO_000628
miriam-gene:4205
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_provenance
{
dgn-np:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_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-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:NP189149.RAxHCmimRJzH7AMNCsaCTp3SVn61XnJlHBnB0KAFpma94130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}