@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc
> .
@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:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_head
{
this:
np:hasAssertion
dgn-np:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_assertion
;
np:hasProvenance
dgn-np:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_provenance
;
np:hasPublicationInfo
dgn-np:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_assertion
a
np:Assertion
.
dgn-np:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_provenance
a
np:Provenance
.
dgn-np:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN47ae49cc087c5c0bf5bc239fe739049b
sio:SIO_000628
miriam-gene:4436
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_provenance
{
dgn-np:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_assertion
dcterms:description
"[Germline mutations in the human DNA mismatch repair (MMR) genes MSH2 and MLH1 are associated with the inherited cancer disorder Lynch syndrome (LS), also known as hereditary nonpolyposis colorectal cancer or HNPCC.]. 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:22753075
;
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:NP994690.RAtDOJNZcRGMJaILXNVPlBCIopICEa1BV6swPJ61XVxMc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:16+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" .
}