@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k
> .
@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:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_head
{
this:
np:hasAssertion
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_assertion
;
np:hasProvenance
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_provenance
;
np:hasPublicationInfo
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_assertion
a
np:Assertion
.
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_provenance
a
np:Provenance
.
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_assertion
{
miriam-gene:11261
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNe3785aef8a23e8dc1f0943b76b7bc832
sio:SIO_000628
miriam-gene:11261
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_provenance
{
dgn-np:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_assertion
dcterms:description
"[To determine the contribution of these genes to the development of basal cell carcinomas we looked for evidence of allelic imbalance in 67 sporadic basal cell carcinoma specimens from Greek patients and screened 28 of them presenting loss of heterozygosity at 9p21-p22 for germline mutations in p16INK4a and p19ARF genes.]. 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:10998150
;
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:NP306626.RA7MiZghwBPpAiUWNm_DM0Pbu7Z2OwwODclkhXDgC767k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}