@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM
> .
@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:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_head
{
this:
np:hasAssertion
dgn-np:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_assertion
;
np:hasProvenance
dgn-np:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_provenance
;
np:hasPublicationInfo
dgn-np:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_assertion
a
np:Assertion
.
dgn-np:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_provenance
a
np:Provenance
.
dgn-np:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0027765
a
ncit:C7057
.
dgn-gda:DGN941d4fc3d5b5850499e5e61b411247ba
sio:SIO_000628
miriam-gene:7276
,
lld:C0027765
;
a
sio:SIO_001121
.
}
dgn-np:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_provenance
{
dgn-np:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_assertion
dcterms:description
"[In the upper limb and facial forms of familial amyloidotic polyneuropathy first recorded in Swiss and Finns respectively, the differences in their patterns of neurological disease and ocular lesions could be the result of their amyloids deriving from proteins other than prealbumin.]. 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:3859886
;
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:NP312769.RA7jXq4hqz-QdHf5_p8TXb4NC3Bkz_WhqJqs1bdEEtrPM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:59+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" .
}