@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU
> .
@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:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_head
{
this:
np:hasAssertion
dgn-np:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_assertion
;
np:hasProvenance
dgn-np:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_provenance
;
np:hasPublicationInfo
dgn-np:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_assertion
a
np:Assertion
.
dgn-np:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_provenance
a
np:Provenance
.
dgn-np:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_assertion
{
miriam-gene:1050
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN086a60814beb6219b5a217709c80250f
sio:SIO_000628
miriam-gene:1050
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_provenance
{
dgn-np:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_assertion
dcterms:description
"[In order to strengthen this hypothesis, we have screened CEBPA for germline mutations in several families presenting aggregation of hematological malignancies (including chronic or acute, lymphoid or myeloid leukemias, Hodgkin's or non Hodgkin's lymphomas, and myeloproliferative or myelodysplastic syndromes) with or without solid tumours.]. 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:19731081
;
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:NP291360.RAhtCHaGnM74a67m2LVMC4ExlhbBCOVvwpgwY9bnDdvrU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}