@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU
> .
@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:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_head
{
this:
np:hasAssertion
dgn-np:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_assertion
;
np:hasProvenance
dgn-np:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_provenance
;
np:hasPublicationInfo
dgn-np:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_assertion
a
np:Assertion
.
dgn-np:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_provenance
a
np:Provenance
.
dgn-np:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGN0043582127ef52fb092db4a5debb7658
sio:SIO_000628
miriam-gene:7276
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_provenance
{
dgn-np:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_assertion
dcterms:description
"[A functional link has been established between the severe neurodegenerative disorder Familial amyloidotic polyneuropathy and the enhanced propensity of the plasma protein transthyretin (TTR) to form aggregates in patients with single point mutations in the TTR gene.]. 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:21179560
;
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:NP767419.RAQuwJyMqAQZvIjxs3foz06VxXSwsWuJSJgmzYC26pXcU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}