@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI
> .
@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:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_head
{
this:
np:hasAssertion
dgn-np:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion
;
np:hasProvenance
dgn-np:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance
;
np:hasPublicationInfo
dgn-np:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion
a
np:Assertion
.
dgn-np:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance
a
np:Provenance
.
dgn-np:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion
{
miriam-gene:2040
a
ncit:C16612
.
lld:C1262483
a
ncit:C7057
.
dgn-gda:DGNdec4b7ca43492a75d9f948d2192a2566
sio:SIO_000628
miriam-gene:2040
,
lld:C1262483
;
a
sio:SIO_001121
.
}
dgn-np:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_provenance
{
dgn-np:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_assertion
dcterms:description
"[The absence of the phenotype of hereditary stomatocytosis implies that protein 7.2b deficiency plays no direct role in the etiology of this disorder and casts doubt on the previously proposed role of this protein as a mediator of cation transport in RBC.]. 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:10090952
;
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:NP853467.RA-cgaVBNWpDlqE8SCkGwdk91KPSK1B9NXYP7-0OxXDkI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:42+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" .
}