@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY
> .
@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:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_head
{
this:
np:hasAssertion
dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_assertion
;
np:hasProvenance
dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_provenance
;
np:hasPublicationInfo
dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_assertion
a
np:Assertion
.
dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_provenance
a
np:Provenance
.
dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_assertion
{
miriam-gene:10923
a
ncit:C16612
.
lld:C0007131
a
ncit:C7057
.
dgn-gda:DGNc356820df7e5d272d1c58bec34214094
sio:SIO_000628
miriam-gene:10923
,
lld:C0007131
;
a
sio:SIO_001121
.
}
dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_provenance
{
dgn-np:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_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:NP261989.RAX6ZKaBHyKFYUYBOU8sDE0zz5mTiN59pW_1VpFvyMmIY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}