@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4
> .
@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:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_head
{
this:
np:hasAssertion
dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_assertion
;
np:hasProvenance
dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_provenance
;
np:hasPublicationInfo
dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_assertion
a
np:Assertion
.
dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_provenance
a
np:Provenance
.
dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1258085
a
ncit:C7057
.
dgn-gda:DGN37657051537af98f7280401c98deac11
sio:SIO_000628
miriam-gene:7157
,
lld:C1258085
;
a
sio:SIO_001121
.
}
dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_provenance
{
dgn-np:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_assertion
dcterms:description
"[Application of these findings to clinical problems include the identification of p53 mutations as markers for malignant change in Barrett's epithelium, the use of discordant p53 mutations to diagnose second primary malignant neoplasms in patients with head and neck cancer, and the potential for therapy by the reversal of genetic lesions.]. 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:1444790
;
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:NP460873.RAvUpf6ha-v9CwB563axtX3qnNb21ti66JJJ30JoDT3s4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:34+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" .
}