@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8
> .
@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:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_head
{
this:
np:hasAssertion
dgn-np:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_assertion
;
np:hasProvenance
dgn-np:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_provenance
;
np:hasPublicationInfo
dgn-np:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_assertion
a
np:Assertion
.
dgn-np:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_provenance
a
np:Provenance
.
dgn-np:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_assertion
{
miriam-gene:5933
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGN2f3d4b7b42c85c96d071fa85dd73d94e
sio:SIO_000628
miriam-gene:5933
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_provenance
{
dgn-np:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_assertion
dcterms:description
"[Our studies suggest that missense mutations in MYC may be selected for during lymphomagenesis, because the mutant MYC proteins have altered functional interactions with p107 protein complexes and fail to be phosphorylated at Thr-58.]. 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:7623799
;
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:NP697780.RAFCSM5yNaYefBYm2LT4HkKQDgwvSSAOdAviktudqjLQ8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}