@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s
> .
@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:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_head
{
this:
np:hasAssertion
dgn-np:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_assertion
;
np:hasProvenance
dgn-np:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_provenance
;
np:hasPublicationInfo
dgn-np:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_assertion
a
np:Assertion
.
dgn-np:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_provenance
a
np:Provenance
.
dgn-np:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0014522
a
ncit:C7057
.
dgn-gda:DGNba16b1aa7af9d853bdeb1d51b731c7a0
sio:SIO_000628
miriam-gene:7157
,
lld:C0014522
;
a
sio:SIO_001121
.
}
dgn-np:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_provenance
{
dgn-np:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_assertion
dcterms:description
"[The arginine variant of the p53 codon 72 polymorphism as well as anogenital and epidermodysplasia verruciformis (EV) types of human papilloma virus (HPV) are suggested to confer increased risk for developing cutaneous squamous cell carcinoma (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:15844633
;
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:NP363458.RA5UbnMAXp0wQeH_uVyVMkmWwXzdJgrgmU_n-og03AN3s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:33+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" .
}