@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk
> .
@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:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_head
{
this:
np:hasAssertion
dgn-np:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_assertion
;
np:hasProvenance
dgn-np:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_provenance
;
np:hasPublicationInfo
dgn-np:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_assertion
a
np:Assertion
.
dgn-np:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_provenance
a
np:Provenance
.
dgn-np:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_assertion
{
miriam-gene:7168
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN0bb260fc7209862f76ebe7746bda9b39
sio:SIO_000628
miriam-gene:7168
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_provenance
{
dgn-np:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_assertion
dcterms:description
"[To prospectively investigate the relationship between myocardial contractile impairment and left ventricular (LV) hypertrophy measured at cardiac magnetic resonance (MR) imaging in patients with hypertrophic cardiomyopathy (HCM) caused by the substitution of aspartic acid 175 with asparagine (ie, Asp175Asn mutation) in the alpha-tropomyosin gene (TPM1).]. 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:16014439
;
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:NP307927.RAvGc0j91wVle-V19SfWaSuwu2QeUzNxbOGHYRFeMwNDk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}