@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs
> .
@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:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_head
{
this:
np:hasAssertion
dgn-np:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_assertion
;
np:hasProvenance
dgn-np:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_provenance
;
np:hasPublicationInfo
dgn-np:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_assertion
a
np:Assertion
.
dgn-np:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_provenance
a
np:Provenance
.
dgn-np:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_assertion
{
miriam-gene:2693
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGN9ad097799fe90ccb12837ff91fd63603
sio:SIO_000628
miriam-gene:2693
,
lld:C0149721
;
a
sio:SIO_001121
.
}
dgn-np:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_provenance
{
dgn-np:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_assertion
dcterms:description
"[These data suggest that common variants in the GHSR region are associated with parameters of LVM and geometry independent of blood pressure and body mass in the general population and, thus, may be involved in the pathogenesis of LVH.]. 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:16567594
;
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:NP440909.RACEjhe8OWz-wX1qOQOHZdtLja5vJ6uc9NG1CGsT8vXAs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}