@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30
> .
@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:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_head
{
this:
np:hasAssertion
dgn-np:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_assertion
;
np:hasProvenance
dgn-np:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_provenance
;
np:hasPublicationInfo
dgn-np:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_assertion
a
np:Assertion
.
dgn-np:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_provenance
a
np:Provenance
.
dgn-np:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_assertion
{
miriam-gene:8991
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN51672007cea63d002a11617e9629072c
sio:SIO_000628
miriam-gene:8991
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_provenance
{
dgn-np:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_assertion
dcterms:description
"[For most measures, the best-fitting model showed no differences in heritability between AAs and EAs or between males and females, with heritabilities of 0.50 for cardiac index, of 0.64 for HR, and of SBP, pulse pressure, and stroke volume in between.]. 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:12719445
;
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:NP279469.RAUyHpmSl44z8vE8o2pntmCYl5CIMkJgZ98OgVOXQDD30130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}