@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM
> .
@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:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_head
{
this:
np:hasAssertion
dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_assertion
;
np:hasProvenance
dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_provenance
;
np:hasPublicationInfo
dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_assertion
a
np:Assertion
.
dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_provenance
a
np:Provenance
.
dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN283ca917c86d14d34f1abdb9d1ded34f
sio:SIO_000628
miriam-gene:4360
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_provenance
{
dgn-np:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_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:NP377772.RA-0LgUrNX0nD2S3LxHLDcLb1Ugo1UlKQcIW0cOlVCBCM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:41+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" .
}