@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_head
{
this:
np:hasAssertion
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_assertion
;
np:hasProvenance
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_assertion
a
np:Assertion
.
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_provenance
a
np:Provenance
.
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_assertion
{
miriam-gene:5313
a
ncit:C16612
.
lld:C1387532
a
ncit:C7057
.
dgn-gda:DGNc370d3cd1d91bc6aa2df3c119d607144
sio:SIO_000628
miriam-gene:5313
,
lld:C1387532
;
a
sio:SIO_001122
.
}
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_provenance
{
dgn-np:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_assertion
dcterms:description
"[ SSCP procedure followed by direct gene sequencing in positive cases is fast and simple enough to allow the identification of PK deficient variants, avoiding the need of biochemical characterisation of semipurified deficient enzyme, which is more cumberso]. 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:10374175
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP80780.RAopE4Bf5ncGKjpingOSiR06zmKvhGSuTbQPrWfcZausQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:24+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}