@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs
> .
@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/v3.0.0/void/
> .
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_head
{
this:
np:hasAssertion
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_assertion
;
np:hasProvenance
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_provenance
;
np:hasPublicationInfo
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_assertion
a
np:Assertion
.
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_provenance
a
np:Provenance
.
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0206246
a
ncit:C7057
.
dgn-gda:DGN0ba4f0725c64ae40670b0b1c242324e6
sio:SIO_000628
miriam-gene:7276
,
lld:C0206246
;
a
sio:SIO_001121
.
}
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_provenance
{
dgn-np:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_assertion
dcterms:description
"[Familial amyloid polyneuropathy (FAP; also known as familiar amyloidosis and hereditary amyloidosis) is an autosomal dominant inherited disease due to mutations of the transthyretin (TTR) gene coding for the corresponding protein, consisting of 127 amino acids.]. 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:23797140
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP761736.RAl4PcdpqW36rSVwuewbSFTxLi1xHUUu9PMLOlkfrcBQs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:19+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}