@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_head
{
this:
np:hasAssertion
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_assertion
;
np:hasProvenance
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_assertion
a
np:Assertion
.
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_provenance
a
np:Provenance
.
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C1321489
a
ncit:C7057
.
dgn-gda:DGNb11aa740d0920a917eebca7fb90c5b24
sio:SIO_000628
miriam-gene:4360
,
lld:C1321489
;
a
sio:SIO_001121
.
}
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_provenance
{
dgn-np:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_assertion
dcterms:description
"[The eponymous Muir-Torre syndrome (MTS) is a clinical variant of hereditary non polyposis colorectal cancer, and is defined as an autosomal dominant condition with simultaneous sebaceous neoplasms of the skin and visceral malignant disease resulting from germline mutations in the DNA mismatch repair (MMR) genes.]. 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:19449129
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP170409.RA1kYbpEA6yv1H63X5BjTErPd1Cs7zWI4SMMjp3iwP7CQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:32+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}