@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc
> .
@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:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_head
{
this:
np:hasAssertion
dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_assertion
;
np:hasProvenance
dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_provenance
;
np:hasPublicationInfo
dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_assertion
a
np:Assertion
.
dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_provenance
a
np:Provenance
.
dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0152025
a
ncit:C7057
.
dgn-gda:DGN2cbd6a2cfacb499d6dcfbb84d3b0f5ee
sio:SIO_000628
miriam-gene:7276
,
lld:C0152025
;
a
sio:SIO_001121
.
}
dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_provenance
{
dgn-np:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_assertion
dcterms:description
"[Clinicians should consider, to avoid misdiagnosis, the screening for TTR mutations in patients presenting with progressive axonal polyneuropathy of undetermined etiology, including apparently sporadic cases with pathological examinations negative for amyloid deposition.]. 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:22592564
;
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:NP761704.RA7sMWsFgCtVQQxQJsi65MMd8ItK2SyNEZbI3XIwVdCOc130_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" .
}