@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys
> .
@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:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_head
{
this:
np:hasAssertion
dgn-np:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_assertion
;
np:hasProvenance
dgn-np:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_provenance
;
np:hasPublicationInfo
dgn-np:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_assertion
a
np:Assertion
.
dgn-np:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_provenance
a
np:Provenance
.
dgn-np:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_assertion
{
miriam-gene:1543
a
ncit:C16612
.
lld:C0220641
a
ncit:C7057
.
dgn-gda:DGNb91b5aa0fc26a9e3a0e2f17fcbc5255c
sio:SIO_000628
miriam-gene:1543
,
lld:C0220641
;
a
sio:SIO_001121
.
}
dgn-np:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_provenance
{
dgn-np:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_assertion
dcterms:description
"[There was a significant association between the prevalence of p53 mutations in oral tumors and CYP1A1 genotyping patterns in these oral cancer patients, with the highest p53 mutation prevalence observed in subjects with the CYP1A1 [val]/GSTM1 [+] genotype (OR = 6.0; CI = 1.2-29.7).]. 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:9525287
;
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:NP287477.RAAmMZeEaQF3fOQQRYHCu3ZIylQ92UGELvsvogb9V6Fys130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:43+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" .
}