@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ
> .
@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:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_head
{
this:
np:hasAssertion
dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_assertion
;
np:hasProvenance
dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_assertion
a
np:Assertion
.
dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_provenance
a
np:Provenance
.
dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN3452ca6aec688958ba381d264681e3c9
sio:SIO_000628
miriam-gene:7276
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_provenance
{
dgn-np:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_assertion
dcterms:description
"[Although TTR mutations were mostly associated with familial amyloid polyneuropathy (FAP), these molecular variants were also found in patients with recurrent stroke, subarachnoidal bleeding and radiological findings of cerebral, cerebellar, cortical-subcortical infarctions and hemosiderosis.]. 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:19428025
;
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:NP737590.RAvLCL6PtYd_HFIdLYLHx-45NJSbvGYtzn3YKK6P7GHPQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:19+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}