@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo
> .
@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:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_head
{
this:
np:hasAssertion
dgn-np:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_assertion
;
np:hasProvenance
dgn-np:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_provenance
;
np:hasPublicationInfo
dgn-np:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_assertion
a
np:Assertion
.
dgn-np:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_provenance
a
np:Provenance
.
dgn-np:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0750974
a
ncit:C7057
.
dgn-gda:DGNe024f09ca22f3bc909fa6e14e328f03d
sio:SIO_000628
miriam-gene:5624
,
lld:C0750974
;
a
sio:SIO_001121
.
}
dgn-np:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_provenance
{
dgn-np:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_assertion
dcterms:description
"[Turcot's syndrome is characterized clinically by the occurrence of primary brain tumor and colorectal tumor and has in previous reports been shown to be associated with germline mutations in the genes APC, hMLH1, and hPMS2.]. 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:10337989
;
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:NP856786.RAThUerJxS26a47sxzMA0zoKyRgxy2Lti05cp4kFCXEqo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:44+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" .
}