@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4
> .
@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:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_head
{
this:
np:hasAssertion
dgn-np:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_assertion
;
np:hasProvenance
dgn-np:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_provenance
;
np:hasPublicationInfo
dgn-np:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_assertion
a
np:Assertion
.
dgn-np:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_provenance
a
np:Provenance
.
dgn-np:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_assertion
{
miriam-gene:6710
a
ncit:C16612
.
lld:C0013902
a
ncit:C7057
.
dgn-gda:DGN7df4a8e88b2a4d1a58f89aa521e3e99a
sio:SIO_000628
miriam-gene:6710
,
lld:C0013902
;
a
sio:SIO_001121
.
}
dgn-np:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_provenance
{
dgn-np:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_assertion
dcterms:description
"[We also investigated methylation profiles in peripheral blood mononuclear cells from patients with red cell membrane diseases, such as complete protein 4.2 deficiency due to ELB42 mutations, hereditary spherocytosis with EPB3 mutations, and hereditary elliptocytosis with SPTB mutations.]. 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:16158818
;
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:NP859873.RAA_AFgcQU-cbN1B2LKxaXqIY3rUQz4CqhHRwftSYiGP4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:45+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" .
}