@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A
> .
@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:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_head
{
this:
np:hasAssertion
dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_assertion
;
np:hasProvenance
dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_assertion
a
np:Assertion
.
dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_provenance
a
np:Provenance
.
dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN9419ff93deee9e6cf02ba342db8af787
sio:SIO_000628
miriam-gene:4292
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_provenance
{
dgn-np:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_assertion
dcterms:description
"[The discovery that mutations occur with equal frequency in MSS and MSI tumors and are most frequent in MSI tumors lacking MLH1 methylation has implications for Lynch syndrome screening and mutation testing.]. 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:25224212
;
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:NP1220404.RA8IvBurkejb6Qa1bhGoDGnE8mzRUbc9ywEZIM37vdn8A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:59+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" .
}