@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ
> .
@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:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_head
{
this:
np:hasAssertion
dgn-np:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_assertion
;
np:hasProvenance
dgn-np:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_assertion
a
np:Assertion
.
dgn-np:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_provenance
a
np:Provenance
.
dgn-np:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_assertion
{
miriam-gene:55743
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGNc40a9e221a2005b64bf683e80485d5be
sio:SIO_000628
miriam-gene:55743
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_provenance
{
dgn-np:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_assertion
dcterms:description
"[However, the p53 mutation was not related to hypermethylation of the CHFR promoter and MIN, which indicates that an abnormality in p53 occurs as an independent process from the mismatch repair deficiency in carcinogenesis.]. 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:19469003
;
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:NP166838.RAYrBK2rJ2A063qJuVUbNn1BcUZioH4JNxOYqHV9gnBiQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}