@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM
> .
@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:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_head
{
this:
np:hasAssertion
dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_assertion
;
np:hasProvenance
dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_provenance
;
np:hasPublicationInfo
dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_assertion
a
np:Assertion
.
dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_provenance
a
np:Provenance
.
dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_assertion
{
miriam-gene:799
a
ncit:C16612
.
lld:C0007847
a
ncit:C7057
.
dgn-gda:DGN48dcf8007f0171b5cd1ee10c73fff9ab
sio:SIO_000628
miriam-gene:799
,
lld:C0007847
;
a
sio:SIO_001121
.
}
dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_provenance
{
dgn-np:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_assertion
dcterms:description
"[The aims of this study were (1) to evaluate the frequency of PIK3CA mutations in patients with cervical cancer treated with radical CRT and (2) to examine the effect of tumor PIK3CA mutational status in pre-treatment biopsies on overall survival (OS) and progression-free survival (PFS).]. 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:23266353
;
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:NP682631.RAH_dhGZM1VPic9M_TmwfDNXT0MAJTSH5h4taLJ3A_vGM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}