@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0
> .
@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:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_head
{
this:
np:hasAssertion
dgn-np:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_assertion
;
np:hasProvenance
dgn-np:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_provenance
;
np:hasPublicationInfo
dgn-np:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_assertion
a
np:Assertion
.
dgn-np:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_provenance
a
np:Provenance
.
dgn-np:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0034887
a
ncit:C7057
.
dgn-gda:DGNcb501225207cf2625baf98bde39ea152
sio:SIO_000628
miriam-gene:324
,
lld:C0034887
;
a
sio:SIO_001121
.
}
dgn-np:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_provenance
{
dgn-np:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_assertion
dcterms:description
"[The higher frequency of LOH in rectal polyps from patients with codon 1309 mutations may help to explain their increased polyp burden at this site compared with patients who have other germline APC mutations.]. 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:20229069
;
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:NP202095.RAk2u8IOxImqRKGMwneTgfM9w4JprcoMGsckO6W-8dZD0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:51+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" .
}