@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik
> .
@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:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_head
{
this:
np:hasAssertion
dgn-np:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_assertion
;
np:hasProvenance
dgn-np:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_provenance
;
np:hasPublicationInfo
dgn-np:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_assertion
a
np:Assertion
.
dgn-np:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_provenance
a
np:Provenance
.
dgn-np:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0018801
a
ncit:C7057
.
dgn-gda:DGNa69161eeaac65b1fc21362cf7cd28e61
sio:SIO_000628
miriam-gene:7276
,
lld:C0018801
;
a
sio:SIO_001121
.
}
dgn-np:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_provenance
{
dgn-np:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_assertion
dcterms:description
"[Cardiac amyloidoses, which are most commonly caused by aggregation of Ig light chains or transthyretin (TTR) in the cardiac interstitium and conducting system, represent an important and often underdiagnosed cause of heart failure.]. 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:23716704
;
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:NP671738.RA-hHvvk-s9NkKwOK3GEwztA1AIEM1IjWvR6FDDQVzFik130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}