@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w
> .
@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:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_head
{
this:
np:hasAssertion
dgn-np:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_assertion
;
np:hasProvenance
dgn-np:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_provenance
;
np:hasPublicationInfo
dgn-np:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_assertion
a
np:Assertion
.
dgn-np:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_provenance
a
np:Provenance
.
dgn-np:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_assertion
{
miriam-gene:3399
a
ncit:C16612
.
lld:C0006413
a
ncit:C7057
.
dgn-gda:DGN56a8a2ca3138cf99eb8068ec109c80d5
sio:SIO_000628
miriam-gene:3399
,
lld:C0006413
;
a
sio:SIO_001121
.
}
dgn-np:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_provenance
{
dgn-np:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_assertion
dcterms:description
"[Two studies in this issue identify the landscape of somatic mutations in Burkitt lymphoma and highlight the pathogenic and clinical relevance of inactivating mutations of ID3, an inhibitor of the TCF3 transcription factor.]. 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:23192177
;
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:NP719022.RAomh4ur4n-B1MOMoWQLcwIkDcfs5FvimZP6Kc7smNg9w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:16+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" .
}