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http://rdf.disgenet.org/nanopublications.trig#NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8130_assertion
a
np:Assertion
.
dgn-np:NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8130_provenance
a
np:Provenance
.
dgn-np:NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8130_assertion
{
miriam-gene:207
a
ncit:C16612
.
lld:C0149925
a
ncit:C7057
.
dgn-gda:DGN6b20204725e8c1082b9e8eae60c5fbb1
sio:SIO_000628
miriam-gene:207
,
lld:C0149925
;
a
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.
}
dgn-np:NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8130_provenance
{
dgn-np:NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8130_assertion
dcterms:description
"[This study for the first time uncovered PIK3CA alterations in SCLC, and our findings suggest that anti-AKT molecular therapy could be effective for a subgroup of SCLC, which shows activation of specific genes, such as PIK3CA mutation, and that genetic stratification of SCLC according to the activation status of individual therapeutic target pathways could be clinically beneficial, especially for chemotherapy-resistant/relapsing tumors.]. 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:19394761
;
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 .
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dgn-np:NP648637.RAR3VznnCFAA87K4Fwei4S9j0PXVaoiSaMR_tdrDeGXl8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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
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pav:authoredBy
<
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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}