@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU
> .
@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:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_head
{
this:
np:hasAssertion
dgn-np:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_assertion
;
np:hasProvenance
dgn-np:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_provenance
;
np:hasPublicationInfo
dgn-np:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_assertion
a
np:Assertion
.
dgn-np:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_provenance
a
np:Provenance
.
dgn-np:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_assertion
{
miriam-gene:1019
a
ncit:C16612
.
lld:C0004114
a
ncit:C7057
.
dgn-gda:DGN46b13e9b33e938f3603e4a08990ad6d3
sio:SIO_000628
miriam-gene:1019
,
lld:C0004114
;
a
sio:SIO_001121
.
}
dgn-np:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_provenance
{
dgn-np:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_assertion
dcterms:description
"[The scarcity of such cases generally requires that molecular analyses of PMAs are based on the utilization of paraffin-embedded material, and here we have used 39 such specimens to examine the incidence and prognostic significance of oncogene and tumor suppressor gene alterations (including amplifications of EGFR, CDK4, and MDM2 as well as inactivating mutations of CDKN2A, TP53, and PTEN) in these 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:10632344
;
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:NP403918.RA2bJyib_gD61nKhsgqMVWwwJrHDdGYR99shs0u7ufvEU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}