@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_head
{
this:
np:hasAssertion
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_assertion
;
np:hasProvenance
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_provenance
;
np:hasPublicationInfo
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_assertion
a
np:Assertion
.
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_provenance
a
np:Provenance
.
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_assertion
{
miriam-gene:4595
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN2ee9aa7b0bdb99543a1e638224b32e18
sio:SIO_000628
miriam-gene:4595
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_provenance
{
dgn-np:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_assertion
dcterms:description
"[Approximately 69% of the excess familial risk in FDRs can be ascribed to MSS CRC, and although the pattern of familial risk supports recessive susceptibility in addition to MUTYH, the absolute risk of CRC is at best modest.]. 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:19307499
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP68009.RAPDhvQGmB1af58ThMpMhkdf5SXpFzM6ZJjKc3EHHM88g130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:17+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}