@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4
> .
@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:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_head
{
this:
np:hasAssertion
dgn-np:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_assertion
;
np:hasProvenance
dgn-np:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_assertion
a
np:Assertion
.
dgn-np:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_provenance
a
np:Provenance
.
dgn-np:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_assertion
{
miriam-gene:10923
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN9259dce3355c2bbc3a15df155290308a
sio:SIO_000628
miriam-gene:10923
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_provenance
{
dgn-np:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_assertion
dcterms:description
"[To understand the association of candidate tumour suppressor genes SH3GL2, p16(INK4a), p14(ARF), and p15(INK4b) in the pathogenesis of head and neck squamous cell carcinoma (HNSCC), we studied the deletion, mutation, and methylation of these genes in 61 dysplastic lesions and 94 HNSCC samples.]. 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:19023882
;
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:NP890907.RAWASaPVQTi2JfEEavaiIo-006IMlRgp-mNuKstiCUhJ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:07+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" .
}