@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI
> .
@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:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_head
{
this:
np:hasAssertion
dgn-np:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_assertion
;
np:hasProvenance
dgn-np:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_provenance
;
np:hasPublicationInfo
dgn-np:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_assertion
a
np:Assertion
.
dgn-np:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_provenance
a
np:Provenance
.
dgn-np:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGN710ad1de51c8390c9e40ccb7d4c3b190
sio:SIO_000628
miriam-gene:4360
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_provenance
{
dgn-np:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_assertion
dcterms:description
"[Lynch syndrome, an autosomal dominant cancer predisposition caused by mutations in DNA mismatch repair (MMR) genes, mainly mainly mutL homolog 1, OMIM 120436 (MLH1) and mutS homolog 2, OMIM 609309 (MSH2), encompasses a tumor spectrum including primarily gastrointestinal, endometrial, and ovarian 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:22034109
;
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:NP934280.RA_q8r52n1VkL6KQZ--6wmh9Twi98z0iUSKaCrJx2hLNI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:48+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" .
}