@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU
> .
@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:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_head
{
this:
np:hasAssertion
dgn-np:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_assertion
;
np:hasProvenance
dgn-np:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_provenance
;
np:hasPublicationInfo
dgn-np:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_assertion
a
np:Assertion
.
dgn-np:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_provenance
a
np:Provenance
.
dgn-np:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_assertion
{
miriam-gene:6584
a
ncit:C16612
.
lld:C0750194
a
ncit:C7057
.
dgn-gda:DGN68a030723e9da255d0885520f2886acf
sio:SIO_000628
miriam-gene:6584
,
lld:C0750194
;
a
sio:SIO_001121
.
}
dgn-np:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_provenance
{
dgn-np:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_assertion
dcterms:description
"[Inducible subjects had more severe left ventricular hypertrophy (LVH) and an increased number of markers of SCD (family history of SCD, syncope or presyncope, fall in systolic blood pressure (BP) during exercise, documented non-sustained VT (NSVT), and marked LVH) compared to non-inducible subjects (IVS 2.4 +/- 0.3 cm vs. 1.6 +/- 0.5 cm, P < 0.001; and two to three vs. one to two markers of SCD, P = 0.007, respectively).]. 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:14734051
;
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:NP647463.RAP1sT-wKTFpzPfIvEAdoqyEIFuj_onS_0UAClh-SrpPU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
<
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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pav:version
"v2.1.0" .
}