@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo
> .
@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/v4.0.0/void/
> .
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_head
{
this:
np:hasAssertion
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_assertion
;
np:hasProvenance
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_provenance
;
np:hasPublicationInfo
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_assertion
a
np:Assertion
.
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_provenance
a
np:Provenance
.
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_assertion
{
miriam-gene:1056
a
ncit:C16612
.
lld:C0206245
a
ncit:C7057
.
dgn-gda:DGN2b56f3b1ff0cd008e0b4389540caf9ed
sio:SIO_000628
miriam-gene:1056
,
lld:C0206245
;
a
sio:SIO_001121
.
}
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_provenance
{
dgn-np:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_assertion
dcterms:description
"[To identify possible factors affecting the psychological impact of pre-symptomatic testing for spinocerebellar ataxia type 2 (SCA2) and familial amyloid polyneuropathy (FAP ATTRV30M), we studied (1) the effect of previous experience with the disease in the family, (2) kinship with the closest affected relative and (3) gender of affected parent, when adapting to test results; as well as (4) differences in the course of psychological wellbeing in 63 subjects ( 28 at-risk for FAP ATTRV30M, and 35 at risk for SCA2), who pursued predictive testing for these diseases, in Cuba and in Portugal.]. 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:19731000
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP761316.RAV80F1WtliOUa9UlKM7PpMmLKo2xQBvP-sSVQ5e6e1Xo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:30+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}