@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE
> .
@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:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_head
{
this:
np:hasAssertion
dgn-np:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_assertion
;
np:hasProvenance
dgn-np:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_provenance
;
np:hasPublicationInfo
dgn-np:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_assertion
a
np:Assertion
.
dgn-np:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_provenance
a
np:Provenance
.
dgn-np:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_assertion
{
miriam-gene:2395
a
ncit:C16612
.
lld:C0949658
a
ncit:C7057
.
dgn-gda:DGN2aab23fc6e8ab25589559da6b1a67d6f
sio:SIO_000628
miriam-gene:2395
,
lld:C0949658
;
a
sio:SIO_001121
.
}
dgn-np:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_provenance
{
dgn-np:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_assertion
dcterms:description
"[The observation that some patients with only mild-to-moderate hypertension exhibit gross left ventricular hypertrophy (LVH) similar to the inherited hypertrophic cardiomyopathies such as familial hypertrophic cardiomyopathy (FHC) and Friedreich's ataxia (FA) has prompted us to investigate the hypothesis that genetic factors associated with excessive myocardial hypertrophy, viz.]. 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:8807151
;
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:NP423002.RAf80zBAG_ML7L_nIKEKTMTxIzupjzXGX8zCm7AAvQvwE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:11+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" .
}