@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y
> .
@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:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_head
{
this:
np:hasAssertion
dgn-np:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_assertion
;
np:hasProvenance
dgn-np:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_assertion
a
np:Assertion
.
dgn-np:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_provenance
a
np:Provenance
.
dgn-np:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_assertion
{
miriam-gene:1056
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN5455c169cd3972590b8583cf5f6078b5
sio:SIO_000628
miriam-gene:1056
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_provenance
{
dgn-np:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_assertion
dcterms:description
"[A constitutional single base pair substitution at codon 1317 was observed in two of the siblings with colorectal cancer, but neither exhibited any colonic features typical of FAP nor an early onset of cancer.]. 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:8834176
;
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:NP779872.RAsLaKcMqhenODPwnVjEXX3XsWH0LUVtwHgXmiLqftk1Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:52+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" .
}