@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q
> .
@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:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_head
{
this:
np:hasAssertion
dgn-np:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_assertion
;
np:hasProvenance
dgn-np:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_assertion
a
np:Assertion
.
dgn-np:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_provenance
a
np:Provenance
.
dgn-np:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_assertion
{
miriam-gene:189
a
ncit:C16612
.
lld:C0003507
a
ncit:C7057
.
dgn-gda:DGNa396031e0c3658fc5cd4d5c9bf10d8af
sio:SIO_000628
miriam-gene:189
,
lld:C0003507
;
a
sio:SIO_001121
.
}
dgn-np:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_provenance
{
dgn-np:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_assertion
dcterms:description
"[Five genetic polymorphisms of the RAAS (ACE, AGTR1, AGT, CMA, CYP11B2) were analyzed in all patients and the results of genetic analysis were correlated to severity of AS and LVH to determine the importance of the polymorphisms for 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:11275936
;
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:NP440816.RAef_Z6uTnim02jZxIphVrQn2XvfvkmsSgiDSoju7f-0Q130_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" .
}