@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI
> .
@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:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_head
{
this:
np:hasAssertion
dgn-np:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_assertion
;
np:hasProvenance
dgn-np:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_provenance
;
np:hasPublicationInfo
dgn-np:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_assertion
a
np:Assertion
.
dgn-np:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_provenance
a
np:Provenance
.
dgn-np:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_assertion
{
miriam-gene:2956
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN90deef367ef1e59df2a90d5a82167e58
sio:SIO_000628
miriam-gene:2956
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_provenance
{
dgn-np:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_assertion
dcterms:description
"[Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder that predisposes to predominantly colorectal and endometrial cancers due to germline mutations in DNA mismatch repair genes, mainly MLH1, MSH2 and in families with excess endometrial cancer also MSH6.]. 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:14961575
;
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:NP431647.RArf06OzuShyvWD5blFDhGs9O_HfUZXTv0rAa_uPFzalI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:01+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" .
}