@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_head
{
this:
np:hasAssertion
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_assertion
;
np:hasProvenance
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_provenance
;
np:hasPublicationInfo
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_assertion
a
np:Assertion
.
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_provenance
a
np:Provenance
.
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_assertion
{
miriam-gene:7139
a
ncit:C16612
.
lld:C0149721
a
ncit:C7057
.
dgn-gda:DGNe439f75b3898153bd3d358069bcc22cb
sio:SIO_000628
miriam-gene:7139
,
lld:C0149721
;
a
sio:SIO_001122
.
}
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_provenance
{
dgn-np:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_assertion
dcterms:description
"[The presence of both the ACE D and AT(1)-R C(1166) allele is associated with LV dilation with systolic dysfunction in genotyped HCM. In addition to the severity of LV hypertrophy, screening for these RAS polymorphisms could contribute to further risk stra]. 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:20975235
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP75086.RAZstpzBOCWNMreKw-VYtet-7Q7jvXIEPSCggwL-4szWY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:21+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}