@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec
> .
@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:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_head
{
this:
np:hasAssertion
dgn-np:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_assertion
;
np:hasProvenance
dgn-np:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_provenance
;
np:hasPublicationInfo
dgn-np:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_assertion
a
np:Assertion
.
dgn-np:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_provenance
a
np:Provenance
.
dgn-np:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNc79d6fc40d53cf4709e2ddea772e6dc0
sio:SIO_000628
miriam-gene:7276
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_provenance
{
dgn-np:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_assertion
dcterms:description
"[The usual constituent amyloid fibril protein is transthyretin (TTR) and the most frequent mutation in the TTR gene associated with FAP (including all Portuguese cases) is that at position 30 (met 30).]. 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:8568528
;
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:NP1346022.RADPWAGwOzJ87c8qPD6Wu7WXb8J0a4bujB5UKFDVWGCec130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:56+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" .
}