@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_assertion
a
np:Assertion
.
dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_provenance
a
np:Provenance
.
dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:1029
a
ncit:C16612
.
lld:C0079474
a
ncit:C7057
.
dgn-gda:DGN1ff22fba9a1b0572354d2730dc88543e
sio:SIO_000628
miriam-gene:1029
,
lld:C0079474
;
a
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.
}
dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_provenance
{
dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_assertion
dcterms:description
"[This is the first description of specific abnormalities in tumor suppressor genes in RDEB associated SCC, and demonstrates that alterations in both p53 and p16ink4a can contribute to RDEB associated SCC.]. 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:15373786
;
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:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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" .
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"v2.1.0" .
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