@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco
> .
@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:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_head
{
this:
np:hasAssertion
dgn-np:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_assertion
;
np:hasProvenance
dgn-np:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_provenance
;
np:hasPublicationInfo
dgn-np:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_assertion
a
np:Assertion
.
dgn-np:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_provenance
a
np:Provenance
.
dgn-np:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_assertion
{
miriam-gene:1056
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNe9c33e57b6002c0d5305d0d1846cc3f6
sio:SIO_000628
miriam-gene:1056
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_provenance
{
dgn-np:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_assertion
dcterms:description
"[The purpose of this study is to develop an early diagnostic method for familial amyloidotic polyneuropathy (FAP) before clinical manifestations appear around the age of 30 yr. Amyloid fibrils isolated from type I FAP (FAP1) of Portuguese, Swedish, and Japanese origins consist of a variant transthyretin (TTR) that contains a methionine-for-valine substitution at position 30 or a mixture of normal TTR and this variant form.]. 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:3457802
;
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:NP245696.RAMV6GDgmGrR6KA3IWkoQgwqnN4jQn7NU75Y80-m8deco130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}