@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE
> .
@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:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_head
{
this:
np:hasAssertion
dgn-np:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_assertion
;
np:hasProvenance
dgn-np:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_provenance
;
np:hasPublicationInfo
dgn-np:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_assertion
a
np:Assertion
.
dgn-np:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_provenance
a
np:Provenance
.
dgn-np:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_assertion
{
miriam-gene:50818
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN92f2ecee65bfb495e7afa35373da9908
sio:SIO_000628
miriam-gene:50818
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_provenance
{
dgn-np:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_assertion
dcterms:description
"[These in vitro results provide an interesting basis for further study into the potential use of SNP for treatment of human gliomas in patients receiving combination therapy with conventional chemotherapeutic agents that exhibit PKC inhibitory activity.]. 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:9506361
;
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:NP707798.RA0zah9di1PqkAnYQCE8ThZ0PQOs_0iFwAc2ct0lHLCsE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}