@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_head
{
this:
np:hasAssertion
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_assertion
;
np:hasProvenance
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_provenance
;
np:hasPublicationInfo
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_assertion
a
np:Assertion
.
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_provenance
a
np:Provenance
.
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN6eb7ded347722de140f8d2abe7912cf4
sio:SIO_000628
miriam-gene:7248
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_provenance
{
dgn-np:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_assertion
dcterms:description
"[Point mutations at the tumour suppressor gene p53 are one of the most frequent genetic alterations in squamous cell carcinoma of the head and neck (SCCHN), which lead to the nuclear accumulation and overexpression of inactive p53 protein.]. 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:9682769
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP759700.RAGU480_OFBHBJcoeoQvBJJriBj7OQlOQaOHgi0ESlJT8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:18+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}