@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc
> .
@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:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_head
{
this:
np:hasAssertion
dgn-np:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_assertion
;
np:hasProvenance
dgn-np:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_provenance
;
np:hasPublicationInfo
dgn-np:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_assertion
a
np:Assertion
.
dgn-np:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_provenance
a
np:Provenance
.
dgn-np:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_assertion
{
miriam-gene:8367
a
ncit:C16612
.
lld:C0175695
a
ncit:C7057
.
dgn-gda:DGNf6f88387ddfac88c6b8efcb74e3f810e
sio:SIO_000628
miriam-gene:8367
,
lld:C0175695
;
a
sio:SIO_001121
.
}
dgn-np:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_provenance
{
dgn-np:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_assertion
dcterms:description
"[To gain insight into the biochemical basis of Sotos syndrome, we tested the ability of each NSD1 PHD domain to bind histone H3 when methylated at regulatory sites Lys4, Lys9, Lys27, Lys36, and Lys79, and histone H4 at regulatory Lys20, and determined whether Sotos point mutations disrupted methylation site-specific binding.]. 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:21972110
;
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:NP904173.RATL5H54V7Lpb0sl2pocigZEgG3BFQSC-sxzSRtznMprc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}