@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c
> .
@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:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_head
{
this:
np:hasAssertion
dgn-np:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_assertion
;
np:hasProvenance
dgn-np:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_provenance
;
np:hasPublicationInfo
dgn-np:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_assertion
a
np:Assertion
.
dgn-np:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_provenance
a
np:Provenance
.
dgn-np:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_assertion
{
miriam-gene:9757
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN02ff1b137cf6c0f20b09cdfe906832a0
sio:SIO_000628
miriam-gene:9757
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_provenance
{
dgn-np:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_assertion
dcterms:description
"[Our work expands the mutation spectrum of MLL2 that may help in better understanding of this molecule, which is important in gene expression, epigenetic control of active chromatin states, embryonic development and cancer.]. 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:22126750
;
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:NP383006.RAR82Z5Hq5eahabBJG3EIb7VdLiYG-PtoQOiTyTBrgI0c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:46+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" .
}