@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I
> .
@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:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_head
{
this:
np:hasAssertion
dgn-np:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_assertion
;
np:hasProvenance
dgn-np:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_provenance
;
np:hasPublicationInfo
dgn-np:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_assertion
a
np:Assertion
.
dgn-np:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_provenance
a
np:Provenance
.
dgn-np:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGNed35b67bc9e389626b248b171e381c17
sio:SIO_000628
miriam-gene:7157
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_provenance
{
dgn-np:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_assertion
dcterms:description
"[Polymorphism in the p53 gene at codon 72 revealed no significant association with the development of CAD or diabetes in Kuwait, which confirms other similar results obtained in the US and Asia.]. 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:16797751
;
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:NP601977.RAOX_6R5k-uns6oiz0950nN9L6ZPYUMN0ZVzeQxNz9B4I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}