@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE
> .
@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:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_head
{
this:
np:hasAssertion
dgn-np:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_assertion
;
np:hasProvenance
dgn-np:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_provenance
;
np:hasPublicationInfo
dgn-np:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_assertion
a
np:Assertion
.
dgn-np:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_provenance
a
np:Provenance
.
dgn-np:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0549473
a
ncit:C7057
.
dgn-gda:DGN1c9ff0f1104986e892404ebb03fef1fd
sio:SIO_000628
miriam-gene:7157
,
lld:C0549473
;
a
sio:SIO_001121
.
}
dgn-np:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_provenance
{
dgn-np:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_assertion
dcterms:description
"[Spontaneous epigenetic mutational events are involved in tumor progression and while radiation increases the absolute prevalence of thyroid cancer in the susceptible it does not increase the rate of p53 mutation and seemingly targets different non-DNA-contact residues than those in spontaneously arising tumors.]. 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:11161841
;
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:NP250728.RAhsQvTOMLqKXfEOR-UMOHyW80i76hI9fe3fkTLjvZopE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}