@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_head
{
this:
np:hasAssertion
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_assertion
;
np:hasProvenance
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_provenance
;
np:hasPublicationInfo
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_assertion
a
np:Assertion
.
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_provenance
a
np:Provenance
.
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_assertion
{
miriam-gene:8766
a
ncit:C16612
.
lld:C0024523
a
ncit:C7057
.
dgn-gda:DGNfc88e11ef1cf638cf31a1006638ea549
sio:SIO_000628
miriam-gene:8766
,
lld:C0024523
;
a
sio:SIO_001121
.
}
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_provenance
{
dgn-np:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_assertion
dcterms:description
"[We observe a similar loss of the subapical enrichment of Rab11a and the kinases and reduced phosphorylation of ezrin in microvillus inclusion disease, which is associated with MYO5B mutations, intestinal microvilli atrophy and malabsorption.]. 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:24413175
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP804771.RAf1oWmMbZB2i_QWO4hj_8rY_Qq6lUbYMch0MQz19P3L0130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:47+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}