@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54
> .
@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:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_head
{
this:
np:hasAssertion
dgn-np:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_assertion
;
np:hasProvenance
dgn-np:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_provenance
;
np:hasPublicationInfo
dgn-np:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_assertion
a
np:Assertion
.
dgn-np:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_provenance
a
np:Provenance
.
dgn-np:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0002726
a
ncit:C7057
.
dgn-gda:DGN0df4225a7139c70b377e496dc646f33f
sio:SIO_000628
miriam-gene:7276
,
lld:C0002726
;
a
sio:SIO_001121
.
}
dgn-np:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_provenance
{
dgn-np:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_assertion
dcterms:description
"[Vitreous amyloidosis is a rare condition that occurs in some forms of Transthyretin hereditary Amyloidosis, mainly in Familial Amyloidotic Polyneuropathy type I. Vitreous opacities may be the earliest occurring or, in some cases, only symptom of this disorder.]. 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:8063479
;
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:NP1331140.RAuaR-kjbZyMXc2pOd9pUZRNzVFd3jq4mVoJBjV7Tms54130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:49+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" .
}