@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE
> .
@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:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_head
{
this:
np:hasAssertion
dgn-np:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_assertion
;
np:hasProvenance
dgn-np:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_provenance
;
np:hasPublicationInfo
dgn-np:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_assertion
a
np:Assertion
.
dgn-np:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_provenance
a
np:Provenance
.
dgn-np:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0009404
a
ncit:C7057
.
dgn-gda:DGN557a369cac235316b7b15b0606da6e03
sio:SIO_000628
miriam-gene:4292
,
lld:C0009404
;
a
sio:SIO_001121
.
}
dgn-np:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_provenance
{
dgn-np:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_assertion
dcterms:description
"[Turcot syndrome is clinically characterized by the occurrence of primary brain tumor and colorectal tumor and has, in previous reports, been shown associated with germline mutations in the genes APC, MLH1, MHS6, and PMS2.]. 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:17389002
;
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:NP932445.RADMzXPxvKwbnrJ0hjcQ7UN6I_tO8SjbaUFEIhzMesAgE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:31+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" .
}