@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo
> .
@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:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_head
{
this:
np:hasAssertion
dgn-np:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_assertion
;
np:hasProvenance
dgn-np:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_provenance
;
np:hasPublicationInfo
dgn-np:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_assertion
a
np:Assertion
.
dgn-np:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_provenance
a
np:Provenance
.
dgn-np:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C0585442
a
ncit:C7057
.
dgn-gda:DGN49d04bcc483c29834be04fa5e5c6cfdd
sio:SIO_000628
miriam-gene:5290
,
lld:C0585442
;
a
sio:SIO_001121
.
}
dgn-np:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_provenance
{
dgn-np:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_assertion
dcterms:description
"[In this largest mutational profiling of osteosarcoma to date, the authors identified for the first time several mutations involving the PI3K pathway, adding osteosarcoma to the growing list of malignancies with PI3K mutations.]. 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:22006429
;
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:NP605866.RA0gxYcnPtmNEDgk65DqB4RJYlXnehZ9_GEBirK5vAtLo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:03+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" .
}