@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg
> .
@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:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_head
{
this:
np:hasAssertion
dgn-np:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_assertion
;
np:hasProvenance
dgn-np:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_provenance
;
np:hasPublicationInfo
dgn-np:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_assertion
a
np:Assertion
.
dgn-np:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_provenance
a
np:Provenance
.
dgn-np:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0018802
a
ncit:C7057
.
dgn-gda:DGN83d7e767b50382cdef35aedf271f26be
sio:SIO_000628
miriam-gene:7276
,
lld:C0018802
;
a
sio:SIO_001121
.
}
dgn-np:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_provenance
{
dgn-np:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_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:NP830633.RARSnJ7YNe-x6h-oyeUOS3CoAX4FGhjPEDIiybL91faGg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}