@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM130_assertion
a
np:Assertion
.
dgn-np:NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM130_provenance
a
np:Provenance
.
dgn-np:NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C1302401
a
ncit:C7057
.
dgn-gda:DGN373f011c9701c15d8a1a4005591481df
sio:SIO_000628
miriam-gene:5624
,
lld:C1302401
;
a
sio:SIO_001121
.
}
dgn-np:NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM130_provenance
{
dgn-np:NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM130_assertion
dcterms:description
"[We have found that FAP patients with germline APC mutations within a small region (codons 1,194-1,392 at most) mainly show allelic loss in their colorectal adenomas, in contrast to other FAP patients, whose 'second hits' tend to occur by truncating mutations in the mutation cluster region.]. 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:10470088
;
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:NP257307.RArboLUud0kGJXKD7M9Dpdv6LgUWbRznVSV1EFZcDzqlM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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
<
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> , <
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> , <
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
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"v2.1.0" .
}