@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y
> .
@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:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_head
{
this:
np:hasAssertion
dgn-np:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_assertion
;
np:hasProvenance
dgn-np:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_assertion
a
np:Assertion
.
dgn-np:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_provenance
a
np:Provenance
.
dgn-np:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_assertion
{
miriam-gene:4609
a
ncit:C16612
.
lld:C0598766
a
ncit:C7057
.
dgn-gda:DGN0e732dd15b620f8568e41782ae323204
sio:SIO_000628
miriam-gene:4609
,
lld:C0598766
;
a
sio:SIO_001121
.
}
dgn-np:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_provenance
{
dgn-np:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_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:NP172631.RApAKYz_bl3B4wC98O5Pt62BmTIC3E1Xcd2Fpp2R34X-Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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
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"v2.1.0" .
}