@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk
> .
@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:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_head
{
this:
np:hasAssertion
dgn-np:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_assertion
;
np:hasProvenance
dgn-np:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_provenance
;
np:hasPublicationInfo
dgn-np:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_assertion
a
np:Assertion
.
dgn-np:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_provenance
a
np:Provenance
.
dgn-np:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_assertion
{
miriam-gene:4595
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN8a0be004fa7e57e29db65aa1cc4c1d5b
sio:SIO_000628
miriam-gene:4595
,
lld:C0009402
;
a
sio:SIO_001122
.
}
dgn-np:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_provenance
{
dgn-np:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_assertion
dcterms:description
"[The Y165C and 1103delC mutations significantly reduce MUTYH protein stability and thus repair activity, whereas the G382D mutation produces dysfunctional protein only suggesting different functional molecular mechanisms by which the MAP phenotype may contribute to the development of CRC.]. 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:15987719
;
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:NP501631.RAtsOSCrhtEs45GZHYmt-NyDBczcvmlL8a2a47BE7Lvlk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:32+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" .
}