@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4
> .
@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:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_head
{
this:
np:hasAssertion
dgn-np:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_assertion
;
np:hasProvenance
dgn-np:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_provenance
;
np:hasPublicationInfo
dgn-np:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_assertion
a
np:Assertion
.
dgn-np:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_provenance
a
np:Provenance
.
dgn-np:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN21325240a82b86529d37ca0a9ee5e4a4
sio:SIO_000628
miriam-gene:4436
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_provenance
{
dgn-np:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_assertion
dcterms:description
"[Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder predisposing to predominantly colorectal cancer (CRC) and endometrial cancer frequently due to germline mutations in DNA mismatch repair (MMR) genes, mainly MLH1, MSH2 and also MSH6 in families seen to demonstrate an excess of endometrial cancer.]. 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:15118395
;
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:NP442150.RAjEybWsgd31SHQe0sWIykVrFJDNvxkBwdUk9gZ1WlUG4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:05+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" .
}