@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE
> .
@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:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_head
{
this:
np:hasAssertion
dgn-np:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_assertion
;
np:hasProvenance
dgn-np:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_provenance
;
np:hasPublicationInfo
dgn-np:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_assertion
a
np:Assertion
.
dgn-np:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_provenance
a
np:Provenance
.
dgn-np:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_assertion
{
miriam-gene:2950
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGN570913f31549801d8586eee044cf5c0a
sio:SIO_000628
miriam-gene:2950
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_provenance
{
dgn-np:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_assertion
dcterms:description
"[As low-penetrance susceptibility genes may combine additively or multiplicatively and contribute to cancer incidence and to the response to chemotherapy, we studied GSTT1, GSTM1, GSTO2, GSTP1 and codon 72 of p53 genotype profiles in ovarian cancer patients.]. 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:16788846
;
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:NP893455.RA0OLx9A8_cHlbpUhTG29JqtklEp7mJd0wEHMjRtJoHeE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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" .
}