@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM
> .
@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:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_head
{
this:
np:hasAssertion
dgn-np:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_assertion
;
np:hasProvenance
dgn-np:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_provenance
;
np:hasPublicationInfo
dgn-np:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_assertion
a
np:Assertion
.
dgn-np:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_provenance
a
np:Provenance
.
dgn-np:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN22610334f277253c4c6031c9e8b1d061
sio:SIO_000628
miriam-gene:7248
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_provenance
{
dgn-np:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_assertion
dcterms:description
"[The impact of codon 72 polymorphism of the human tumour suppressor gene p53 on the risk of developing squamous cell carcinomas of the head and neck (HNSCC) remains unclear because of contradictory results found by several studies.]. 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:17970074
;
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:NP160702.RAN7Gz8fnJO4BiExmWsrehcRojMtkLzONR5XsDxoVIUBM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}