@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g
> .
@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:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_head
{
this:
np:hasAssertion
dgn-np:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_assertion
;
np:hasProvenance
dgn-np:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_provenance
;
np:hasPublicationInfo
dgn-np:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_assertion
a
np:Assertion
.
dgn-np:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_provenance
a
np:Provenance
.
dgn-np:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0007129
a
ncit:C7057
.
dgn-gda:DGN3dfdf27e432b96e045b489d425376be7
sio:SIO_000628
miriam-gene:7248
,
lld:C0007129
;
a
sio:SIO_001121
.
}
dgn-np:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_provenance
{
dgn-np:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_assertion
dcterms:description
"[In view of the occurrence of 1p deletions in Merkel cell carcinoma (MCC) and the location of p73 we decided to search for mutations in the p73 gene in five MCC cell lines and ten MCC tumours to test potential tumour suppressor function for this gene in MCC.]. 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:10732753
;
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:NP308726.RA4C4j1iOFQw1x5PpR3qX_MzypRcqSc5yBANYJ7Dc3M3g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}