@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA
> .
@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:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_head
{
this:
np:hasAssertion
dgn-np:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_assertion
;
np:hasProvenance
dgn-np:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_provenance
;
np:hasPublicationInfo
dgn-np:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_assertion
a
np:Assertion
.
dgn-np:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_provenance
a
np:Provenance
.
dgn-np:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C0025286
a
ncit:C7057
.
dgn-gda:DGNa71db18f99d3b68c0826d1e5841c21e0
sio:SIO_000628
miriam-gene:1499
,
lld:C0025286
;
a
sio:SIO_001121
.
}
dgn-np:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_provenance
{
dgn-np:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_assertion
dcterms:description
"[We used polymerase chain reaction PCR and direct sequencing methods to investigate whether mutations in the CTNNB1 phosphorylation sites S33, S37, S41 and T45 were present in 68 brain tumours, including meningioma, astrocytoma, pituitary adenoma, neuroblastoma, metastasis to the brain, and cell lines.]. 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:19582367
;
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:NP588112.RAuqupbOxbkseVZu9XQre2h0OXzSlQLr9uKmZUFVUpNFA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}