@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60
> .
@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:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_head
{
this:
np:hasAssertion
dgn-np:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_assertion
;
np:hasProvenance
dgn-np:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_provenance
;
np:hasPublicationInfo
dgn-np:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_assertion
a
np:Assertion
.
dgn-np:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_provenance
a
np:Provenance
.
dgn-np:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_assertion
{
miriam-gene:4595
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGNfa0f90177a65bd2363ab1f8e83b7a765
sio:SIO_000628
miriam-gene:4595
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_provenance
{
dgn-np:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_assertion
dcterms:description
"[In 26% of these patients, an MUTYH mutation was identified and the detection rate increased with the number of adenomas, irrespectively of family history, being significantly higher in MCRA patients presenting more than 30 adenomas [7/12 (58%) vs 2/14 (14%), p = 0.023].]. 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:19793053
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP579898.RAL6NJkMMyikkTZS5-AU56P7qqtgpOWMGPZFDYZ3VEL60130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:25+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" .
}