@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU
> .
@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:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_head
{
this:
np:hasAssertion
dgn-np:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_assertion
;
np:hasProvenance
dgn-np:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_provenance
;
np:hasPublicationInfo
dgn-np:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_assertion
a
np:Assertion
.
dgn-np:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_provenance
a
np:Provenance
.
dgn-np:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_assertion
{
miriam-gene:1373
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGN50417a5c1bb94b4746b2245faad097b3
sio:SIO_000628
miriam-gene:1373
,
lld:C0014544
;
a
sio:SIO_001122
.
}
dgn-np:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_provenance
{
dgn-np:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_assertion
dcterms:description
"[These findings suggested that in epileptic patients undergoing VPA therapy, CPS14217A polymorphism and the number of coadministered anticonvulsants would be considered as risk factors for hyperammonemia, even if the serum VPA concentrations were controlle]. 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:20456087
;
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:NP143382.RAW32GsEmAiD-4rys4NZ8tB33LNvHTZV5md6gd57q0rYU130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:39:00+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" .
}