@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck
> .
@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:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_head
{
this:
np:hasAssertion
dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_assertion
;
np:hasProvenance
dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_provenance
;
np:hasPublicationInfo
dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_assertion
a
np:Assertion
.
dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_provenance
a
np:Provenance
.
dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_assertion
{
miriam-gene:3251
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGN19e0e9b532b70e89f1c02c7bf3347af3
sio:SIO_000628
miriam-gene:3251
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_provenance
{
dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_assertion
dcterms:description
"[We demonstrated that, in a limited number of colonies from an ovarian cancer, there was an ability to increase the mutation frequency at the HPRT locus after exposure to common chemotheraputics used in the treatment of this disease.]. 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:16158952
;
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:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}