@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg
> .
@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:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_head
{
this:
np:hasAssertion
dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_assertion
;
np:hasProvenance
dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_provenance
;
np:hasPublicationInfo
dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_assertion
a
np:Assertion
.
dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_provenance
a
np:Provenance
.
dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN88c3ae96ef4aafdd47c749f245970065
sio:SIO_000628
miriam-gene:4292
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_provenance
{
dgn-np:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_assertion
dcterms:description
"[Due to the minor role of germline MSH6 mutations, we adapted the Lynch syndrome detection strategy for the Slovenian population of CRC patients, whereby germline alterations should be first sought in MLH1 and MSH2 followed by a search for larger genomic rearrangements in these two genes.]. 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:19526325
;
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:NP745340.RAU37RbyNNbIIB7dizrMxaE9yCtydl8Kr7nRnF0Q7H8Eg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:23+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" .
}