@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc
> .
@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:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_head
{
this:
np:hasAssertion
dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_assertion
;
np:hasProvenance
dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_provenance
;
np:hasPublicationInfo
dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_assertion
a
np:Assertion
.
dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_provenance
a
np:Provenance
.
dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN8e379806b432de2b09564e4aa82aaf70
sio:SIO_000628
miriam-gene:7157
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_provenance
{
dgn-np:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_assertion
dcterms:description
"[We genotyped p53 codon 72 in 193 individuals with Lynch syndrome mutations, 93 patients with sporadic microsatellite unstable colorectal cancer, and 93 patients with sporadic microsatellite stable colorectal cancer from Finland and 323 Finnish controls.]. 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:16203772
;
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:NP156975.RAIoopm0-E3l1-6j3j02mOPVwrHLt7LsBHXX_S9K4Ibkc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:24+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" .
}