@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE
> .
@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:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_head
{
this:
np:hasAssertion
dgn-np:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_assertion
;
np:hasProvenance
dgn-np:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_provenance
;
np:hasPublicationInfo
dgn-np:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_assertion
a
np:Assertion
.
dgn-np:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_provenance
a
np:Provenance
.
dgn-np:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0878544
a
ncit:C7057
.
dgn-gda:DGNb114f83e71f9ec693d6cef95f4055f04
sio:SIO_000628
miriam-gene:183
,
lld:C0878544
;
a
sio:SIO_001121
.
}
dgn-np:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_provenance
{
dgn-np:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_assertion
dcterms:description
"[Results indicate that the ACE I/D and angiotensinogen M235T and T174M polymorphisms are not related to HCM or DCM in the Japanese population, and that variants of these polymorphisms do not contribute to the genesis or progression of these cardiomyopathies.]. 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:9270088
;
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:NP677100.RAwnjoOsAZzaq-xqzKk1BzIJDStR9PFGkhfKK7QKv7diE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}