@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs
> .
@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:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_head
{
this:
np:hasAssertion
dgn-np:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_assertion
;
np:hasProvenance
dgn-np:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_provenance
;
np:hasPublicationInfo
dgn-np:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_assertion
a
np:Assertion
.
dgn-np:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_provenance
a
np:Provenance
.
dgn-np:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_assertion
{
miriam-gene:1144
a
ncit:C16612
.
lld:C0751885
a
ncit:C7057
.
dgn-gda:DGNf32eb75bf49ce7c0ba6ac60f28b87c87
sio:SIO_000628
miriam-gene:1144
,
lld:C0751885
;
a
sio:SIO_001121
.
}
dgn-np:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_provenance
{
dgn-np:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_assertion
dcterms:description
"[Because levels of quinidine sulfate attainable in clinical practice shorten the opening episodes of genetically engineered mutant SCCMS receptors in vitro, we tested the notion that the drug can be of benefit in SCCMS.]. 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:9546329
;
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:NP628901.RAM4TuS7NkeIYJcQR5D9hblYS_5UHMx11oju2xCeVSKcs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:19+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" .
}