@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA
> .
@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:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_head
{
this:
np:hasAssertion
dgn-np:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_assertion
;
np:hasProvenance
dgn-np:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance
;
np:hasPublicationInfo
dgn-np:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_assertion
a
np:Assertion
.
dgn-np:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance
a
np:Provenance
.
dgn-np:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_assertion
{
miriam-gene:51119
a
ncit:C16612
.
lld:C0037889
a
ncit:C7057
.
dgn-gda:DGN83fd519b907ef12d8d742f6808e3d276
sio:SIO_000628
miriam-gene:51119
,
lld:C0037889
;
a
sio:SIO_001121
.
}
dgn-np:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_provenance
{
dgn-np:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_assertion
dcterms:description
"[Erythrocyte ghosts from eight individuals with hereditary spherocytosis have been compared with respect to their protein compositions as judged by SDS gel electrophoresis, their ease of spectrin extractability, and their freeze-etch electron microscopic appearance after incubation in condition designed to promote aggregation of the intramembrane particles.]. 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:6849841
;
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:NP827193.RADMpY1NgE0ILlH7YcaLBpP7gVGcx80-HYOGBvKg4dgVA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:26+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" .
}