@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE
> .
@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:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_head
{
this:
np:hasAssertion
dgn-np:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_assertion
;
np:hasProvenance
dgn-np:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_provenance
;
np:hasPublicationInfo
dgn-np:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_assertion
a
np:Assertion
.
dgn-np:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_provenance
a
np:Provenance
.
dgn-np:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNa687630ead3c86794a723330ab252eff
sio:SIO_000628
miriam-gene:1499
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_provenance
{
dgn-np:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_assertion
dcterms:description
"[Unusual messenger RNA splicing and missense mutations in the beta-catenin gene (CTNNB1) that result in stabilization of the protein were identified in six of the lines, and the adenomatous polyposis coli tumor suppressor protein (APC) was altered or missing in two others.]. 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:9065403
;
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:NP446477.RAIFx9TNWfV9cUDd5kKoyhyuPG5KMwBk756JqBeL838xE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:26+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" .
}