@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc
> .
@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:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_head
{
this:
np:hasAssertion
dgn-np:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_assertion
;
np:hasProvenance
dgn-np:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_provenance
;
np:hasPublicationInfo
dgn-np:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_assertion
a
np:Assertion
.
dgn-np:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_provenance
a
np:Provenance
.
dgn-np:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0333983
a
ncit:C7057
.
dgn-gda:DGN6ef338afeb386451bd2b84d6bf9e973e
sio:SIO_000628
miriam-gene:5624
,
lld:C0333983
;
a
sio:SIO_001121
.
}
dgn-np:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_provenance
{
dgn-np:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_assertion
dcterms:description
"[In this study, 46 serrated adenomas from 39 patients, 32 conventional (nonserrated) adenomas from 31 patients, and 18 hyperplastic polyps from 16 patients were evaluated for loss of heterozygosity (LOH) of APC, p53, p16, and 3p and for K-ras mutations of codons 12, 13, and 61 by polymerase chain reaction (PCR) analysis.]. 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:11823977
;
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:NP228057.RA1cvcJtCh-M4caRIy6cdPJeIviQXGlFhV0wwa_uC9Uwc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}