@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY
> .
@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:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_head
{
this:
np:hasAssertion
dgn-np:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_assertion
;
np:hasProvenance
dgn-np:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_assertion
a
np:Assertion
.
dgn-np:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_provenance
a
np:Provenance
.
dgn-np:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_assertion
{
miriam-gene:2956
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNa1d769bc924e78e7b92eccf99026fa8e
sio:SIO_000628
miriam-gene:2956
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_provenance
{
dgn-np:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_assertion
dcterms:description
"[Using a multimodal approach, we have identified mutations in MLH1, MSH2, and MSH6 in French Canadian families fulfilling the Amsterdam criteria for Lynch syndrome and who displayed abnormal staining for at least one of the Lynch syndrome proteins.]. 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:19459153
;
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:NP740355.RAC5SvPMlsf60aKnl9KbbWHCTfLkgG5oLji01QCPD3TUY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:20+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" .
}