@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM
> .
@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:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_head
{
this:
np:hasAssertion
dgn-np:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_assertion
;
np:hasProvenance
dgn-np:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_provenance
;
np:hasPublicationInfo
dgn-np:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_assertion
a
np:Assertion
.
dgn-np:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_provenance
a
np:Provenance
.
dgn-np:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_assertion
{
miriam-gene:7168
a
ncit:C16612
.
lld:C0007194
a
ncit:C7057
.
dgn-gda:DGN7fb2d7f26db7038e9483144e727148ed
sio:SIO_000628
miriam-gene:7168
,
lld:C0007194
;
a
sio:SIO_001121
.
}
dgn-np:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_provenance
{
dgn-np:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_assertion
dcterms:description
"[The present study was conducted to investigate the association of N-terminal pro-B-type natriuretic peptide (NT-pro-BNP) levels with LV remodeling on magnetic resonance imaging and procollagen formation in 17 healthy controls and 24 patients with nonobstructive HC attributable to an identical Asp175Asn (aspartic acid to asparagine at codon 175) mutation in the alpha-tropomyosin gene.]. 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:18394456
;
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:NP298915.RAw2hqYaVmTpT2Wsw-4xOdpbx13337NwfUshG12COC6nM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}