@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes
> .
@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:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_head
{
this:
np:hasAssertion
dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_assertion
;
np:hasProvenance
dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_provenance
;
np:hasPublicationInfo
dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_assertion
a
np:Assertion
.
dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_provenance
a
np:Provenance
.
dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN5fb09c8e98c7255c016a73a64ec58779
sio:SIO_000628
miriam-gene:5624
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_provenance
{
dgn-np:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_assertion
dcterms:description
"[Analyses included completion of APC gene exon 16 sequencing, analysis for APC gene copy number variations (deletions or duplications), MUTYH gene sequencing, and microsatellite instability in CRC patients fulfilling Bethesda (laboratory investigation) criteria for Lynch syndrome.]. 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:21287799
;
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:NP869642.RA6ewRRpc9squw6gk0XxhFcW--q2biAqKMI3cnvo1Mqes130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:18+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" .
}