@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac
> .
@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:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_head
{
this:
np:hasAssertion
dgn-np:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_assertion
;
np:hasProvenance
dgn-np:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_provenance
;
np:hasPublicationInfo
dgn-np:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_assertion
a
np:Assertion
.
dgn-np:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_provenance
a
np:Provenance
.
dgn-np:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_assertion
{
miriam-gene:5291
a
ncit:C16612
.
lld:C0007103
a
ncit:C7057
.
dgn-gda:DGNbe35ff180e9906c077b3d9381f5f9376
sio:SIO_000628
miriam-gene:5291
,
lld:C0007103
;
a
sio:SIO_001121
.
}
dgn-np:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_provenance
{
dgn-np:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_assertion
dcterms:description
"[The results affirm the utility of systematic characterization of the cancer genome in clinically annotated specimens and suggest the particular importance of the PI3K pathway in patients who have aggressive endometrial cancer.]. 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:19261849
;
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:NP766798.RAXbbuA9rnxHwevI6VG17MZUDkZN26lv15-LiDtwTStac130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}