@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794
> .
@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:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_head
{
this:
np:hasAssertion
dgn-np:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_assertion
;
np:hasProvenance
dgn-np:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_provenance
;
np:hasPublicationInfo
dgn-np:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_assertion
a
np:Assertion
.
dgn-np:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_provenance
a
np:Provenance
.
dgn-np:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0151546
a
ncit:C7057
.
dgn-gda:DGNcfbf9f3102c123c002d32b66c46de22d
sio:SIO_000628
miriam-gene:7248
,
lld:C0151546
;
a
sio:SIO_001121
.
}
dgn-np:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_provenance
{
dgn-np:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_assertion
dcterms:description
"[DNA technology, especially allelic imbalance (loss of heterozygosity) studies have identified chromosomal changes in oral carcinoma and head and neck squamous cell carcinoma (SCCHN), suggestive of the involvement of tumour suppressor genes (TSGs), particularly in chromosomes 3, 9, 11 and 17.]. 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:10899669
;
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:NP237406.RAYcI86q-__P8MvAWLKPsCfqOaX9R6soyvNv78VlE6794130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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" .
}