@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY
> .
@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:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_head
{
this:
np:hasAssertion
dgn-np:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_assertion
;
np:hasProvenance
dgn-np:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_provenance
;
np:hasPublicationInfo
dgn-np:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_assertion
a
np:Assertion
.
dgn-np:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_provenance
a
np:Provenance
.
dgn-np:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_assertion
{
miriam-gene:5132
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN876c745de3c0e5af1a968d5c5db7b135
sio:SIO_000628
miriam-gene:5132
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_provenance
{
dgn-np:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_assertion
dcterms:description
"[The breakpoints in uterine leiomyomata would fall in the NH2-terminal portion of the protein between a conserved domain found in histones H1 and H5 and the PHD zinc fingers, the CH2CH zinc finger, or the CoA binding site, which is distinct from the breakpoints reported in AML.]. 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:15313893
;
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:NP200609.RAhF6q-3VJDPYF3NV9oGY1Hb2cgac8pOh60efedk-i4JY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}