@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U
> .
@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:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_head
{
this:
np:hasAssertion
dgn-np:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_assertion
;
np:hasProvenance
dgn-np:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_provenance
;
np:hasPublicationInfo
dgn-np:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_assertion
a
np:Assertion
.
dgn-np:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_provenance
a
np:Provenance
.
dgn-np:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_assertion
{
miriam-gene:133418
a
ncit:C16612
.
lld:C1449563
a
ncit:C7057
.
dgn-gda:DGNb3287f459ef545d7a9c7c6dca4058dd5
sio:SIO_000628
miriam-gene:133418
,
lld:C1449563
;
a
sio:SIO_001121
.
}
dgn-np:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_provenance
{
dgn-np:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_assertion
dcterms:description
"[Clinical and biochemical evaluation, right ventricular endomyocardial biopsy (EMB), light and electron microscopic and immunohistochemical studies of biopsy samples, six multiplex and two single polymerase chain reactions for 38 exons and automated sequencing of exon 9 and muscle promoter-exon 1 were undertaken in 201 consecutive male patients presenting with DCM, with (n = 14) and without (n = 187) increased serum creatine phosphokinase (sCPK).]. 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:10841222
;
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:NP557873.RAM0hTdNhJt5wd0vv1VTYwS90lHyYpenLWb7wsmxX1l0U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}