@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ
> .
@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:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_head
{
this:
np:hasAssertion
dgn-np:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_assertion
;
np:hasProvenance
dgn-np:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_assertion
a
np:Assertion
.
dgn-np:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_provenance
a
np:Provenance
.
dgn-np:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0268407
a
ncit:C7057
.
dgn-gda:DGNe8a94649b957a1591bd627c3782e8d14
sio:SIO_000628
miriam-gene:7276
,
lld:C0268407
;
a
sio:SIO_001121
.
}
dgn-np:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_provenance
{
dgn-np:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_assertion
dcterms:description
"[The following were performed: genotyping of banked DNA for TTR V122I allele status and review of cardiovascular and demographic parameters in CHS and ARIC databases, with statistical comparisons of the frequency of congestive heart failure, survival, and occurrence of features of cardiac amyloidosis in carriers of the amyloidogenic allele and controls.]. 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:20435197
;
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:NP226176.RA7DjzjNrdw9d3fxUjenFfv6NeGzzba57KCJx_8sz4dfQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}