@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc
> .
@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:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_head
{
this:
np:hasAssertion
dgn-np:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_assertion
;
np:hasProvenance
dgn-np:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_provenance
;
np:hasPublicationInfo
dgn-np:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_assertion
a
np:Assertion
.
dgn-np:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_provenance
a
np:Provenance
.
dgn-np:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNa1dee56c5d5c6d0c9d60bf4f57d33eca
sio:SIO_000628
miriam-gene:1437
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_provenance
{
dgn-np:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_assertion
dcterms:description
"[To perform qualitative analysis of variant TTR in CSF of patients who underwent a sequential liver transplantation using an explanted familial amyloidotic polyneuropathy (FAP) ATTR Val30 Met patient's liver, levels and forms of TTR of the two patients were analyzed by means of enzyme linked immunosorbent assay (ELISA) and matrix-assisted laser desorption/time-of-flight mass spectrometer (MALDI/TOF-MS), respectively.]. 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:11477356
;
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:NP195948.RANNODD4aDrVgV-DoSj1KfTxBaT2e8TC6sTeo2IYtGMOc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:48+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" .
}