@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4
> .
@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:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_head
{
this:
np:hasAssertion
dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_assertion
;
np:hasProvenance
dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_assertion
a
np:Assertion
.
dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_provenance
a
np:Provenance
.
dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_assertion
{
miriam-gene:4595
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNab3c66aa5fdc42ff7f9e8f209b506867
sio:SIO_000628
miriam-gene:4595
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_provenance
{
dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_assertion
dcterms:description
"[Biallelic germline mutations of MUTYH have been shown to predict familial and sporadic multiple colorectal adenomas and carcinomas, however, whether there is an association between single nucleotide polymorphisms (SNPs) of MUTYH and sporadic colorectal cancer (CRC) risk has remained unclear.]. 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:18271935
;
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:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:33+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" .
}