@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0
> .
@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:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_head
{
this:
np:hasAssertion
dgn-np:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_assertion
;
np:hasProvenance
dgn-np:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_provenance
;
np:hasPublicationInfo
dgn-np:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_assertion
a
np:Assertion
.
dgn-np:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_provenance
a
np:Provenance
.
dgn-np:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_assertion
{
miriam-gene:2703
a
ncit:C16612
.
lld:C0023976
a
ncit:C7057
.
dgn-gda:DGN3cfe46e342dc437a0f8c1d4fe135f6e6
sio:SIO_000628
miriam-gene:2703
,
lld:C0023976
;
a
sio:SIO_001121
.
}
dgn-np:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_provenance
{
dgn-np:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_assertion
dcterms:description
"[A method for automated dideoxy fingerprinting (ddF) using capillary array electrophoresis (CAE) was developed and the efficiency of the method was tested by analyzing 24 DNA samples with mutations in one of the genes KCNQ1 and KCNH2, which are involved in 50% of LQTS cases.]. 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:11668638
;
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:NP652168.RAKTGlMdCK-2dVI21KjYqpvDwHKaJXdH_rbbrL34DxBn0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}