@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE
> .
@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:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_head
{
this:
np:hasAssertion
dgn-np:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_assertion
;
np:hasProvenance
dgn-np:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_provenance
;
np:hasPublicationInfo
dgn-np:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_assertion
a
np:Assertion
.
dgn-np:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_provenance
a
np:Provenance
.
dgn-np:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_assertion
{
miriam-gene:10263
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGN3b80d654c7e10a215660b1c26548de96
sio:SIO_000628
miriam-gene:10263
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_provenance
{
dgn-np:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_assertion
dcterms:description
"[We have analyzed EGFR and HER2 mutations and the expression of the two products of the CDKN2A gene (p14(arf) and p16(INK4a)) in 116 NSCLC that have been previously analyzed for TP53 and KRAS mutations in relation to smoking history of patients.]. 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:17575133
;
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:NP823589.RAtW53ECg6OWPkkiSCOvdmhTlCbtGMkEydylrwPjD1vBE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:24+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" .
}