@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g
> .
@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:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_head
{
this:
np:hasAssertion
dgn-np:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_assertion
;
np:hasProvenance
dgn-np:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_provenance
;
np:hasPublicationInfo
dgn-np:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_assertion
a
np:Assertion
.
dgn-np:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_provenance
a
np:Provenance
.
dgn-np:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C0334108
a
ncit:C7057
.
dgn-gda:DGN7e09b81a21904afc5a8bacd86db4a3b5
sio:SIO_000628
miriam-gene:4436
,
lld:C0334108
;
a
sio:SIO_001121
.
}
dgn-np:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_provenance
{
dgn-np:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_assertion
dcterms:description
"[Hereditary non-polyposis colorectal cancer is the most common known genetic syndrome that predisposes to various types of cancer including gastric cancer and occures mainly due to pathogenic germline mutations in DNA mismatch repair (MMR) genes, such as MLH1, MSH2 and 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:21136174
;
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:NP857393.RAlFa8VAWnj7b6RUDAeVflqDk1r_zOC8RKDME-gfFCB6g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:13+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" .
}