@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc
> .
@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:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_head
{
this:
np:hasAssertion
dgn-np:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_assertion
;
np:hasProvenance
dgn-np:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_provenance
;
np:hasPublicationInfo
dgn-np:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_assertion
a
np:Assertion
.
dgn-np:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_provenance
a
np:Provenance
.
dgn-np:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_assertion
{
miriam-gene:4595
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGN0f467a08b97ebceecef220087769d8ac
sio:SIO_000628
miriam-gene:4595
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_provenance
{
dgn-np:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_assertion
dcterms:description
"[MUTYH-associated polyposis is an autosomal recessively inherited disease which has clinical overlap with Familial adenomatous polyposis and its attenuated form, in that it is associated with risk of colon cancer at a young age.]. 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:20625837
;
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:NP624806.RA2V77jwTgSmWBy2idWwQnim1iiFirt-_hweth4wLlwrc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:17+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" .
}