@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4
> .
@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:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_head
{
this:
np:hasAssertion
dgn-np:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_assertion
;
np:hasProvenance
dgn-np:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_provenance
;
np:hasPublicationInfo
dgn-np:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_assertion
a
np:Assertion
.
dgn-np:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_provenance
a
np:Provenance
.
dgn-np:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGNf73f5df1d3ed1c6b10ce378ba100c7b8
sio:SIO_000628
miriam-gene:133482
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_provenance
{
dgn-np:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_assertion
dcterms:description
"[The authors of this report hypothesized that patients with anaplastic glioma (AG) who have GST genotypes that encode for lower activity enzymes will have longer survival than similar patients who have higher activity genotypes.]. 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:20187096
;
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:NP306001.RAHX70T2TP9_LIbBC5Hs4goNf4MtvaIDlrJ6tIqTeprM4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}