@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc
> .
@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:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_head
{
this:
np:hasAssertion
dgn-np:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_assertion
;
np:hasProvenance
dgn-np:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_provenance
;
np:hasPublicationInfo
dgn-np:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_assertion
a
np:Assertion
.
dgn-np:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_provenance
a
np:Provenance
.
dgn-np:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_assertion
{
miriam-gene:100038246
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGNbf3257973d44f47538bb5506221d61c3
sio:SIO_000628
miriam-gene:100038246
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_provenance
{
dgn-np:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_assertion
dcterms:description
"[Systolic (Sa) and diastolic (Ea) myocardial velocities measured by tissue Doppler (TD) imaging (TDI) recently were shown to be decreased in subjects who have mutations causing hypertrophic cardiomyopathy (HCM) but who do not have left ventricular (LV) hypertrophy.]. 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:12860897
;
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:NP608156.RACYNQAACYIpo6nsrd_r1dN8M-92oXTX1B7Y7ghoD8zDc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}