@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk
> .
@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:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_head
{
this:
np:hasAssertion
dgn-np:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_assertion
;
np:hasProvenance
dgn-np:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_provenance
;
np:hasPublicationInfo
dgn-np:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_assertion
a
np:Assertion
.
dgn-np:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_provenance
a
np:Provenance
.
dgn-np:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNfb35350563c146e0deea2fdea79c6acd
sio:SIO_000628
miriam-gene:1499
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_provenance
{
dgn-np:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_assertion
dcterms:description
"[ CTNNB1 mutations seem to be of minor importance in sporadic colorectal cancer. The main differences in tumour and patient characteristics are found between groups of patients based on mismatch repair deficiency.]. 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:16356174
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP46398.RAPhc6VN4jK2fw6_DougIcV9gna72gFD6pS79T07bvPyk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}