@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE
> .
@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/v4.0.0/void/
> .
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_head
{
this:
np:hasAssertion
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_assertion
;
np:hasProvenance
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_provenance
;
np:hasPublicationInfo
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_assertion
a
np:Assertion
.
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_provenance
a
np:Provenance
.
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_assertion
{
miriam-gene:2956
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNdf9be0fee5e8d6ad664ee95250609185
sio:SIO_000628
miriam-gene:2956
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_provenance
{
dgn-np:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_assertion
dcterms:description
"[CRC patients carrying monoallelic MUTYH mutations harbor more frequently concomitant MSH6 mutations than patients without them, thus suggesting that both genes could act cooperatively and confer together an increased CRC risk.]. 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:19685280
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP757952.RANkYMUefnD7it10TaJZ4t58R2Ib3UIVSf4s4gDbPOBNE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:28+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}