@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8
> .
@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:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_head
{
this:
np:hasAssertion
dgn-np:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_assertion
;
np:hasProvenance
dgn-np:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_provenance
;
np:hasPublicationInfo
dgn-np:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_assertion
a
np:Assertion
.
dgn-np:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_provenance
a
np:Provenance
.
dgn-np:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_assertion
{
miriam-gene:7167
a
ncit:C16612
.
lld:C0149676
a
ncit:C7057
.
dgn-gda:DGN1a24a89fb0d6f2d00b095d896e34f788
sio:SIO_000628
miriam-gene:7167
,
lld:C0149676
;
a
sio:SIO_001121
.
}
dgn-np:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_provenance
{
dgn-np:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_assertion
dcterms:description
"[The striking difference in the clinical course of the defect between the two brothers with the same severe red blood cell enzyme deficiency may originate from unusual differences between two double heterozygous brothers resulting inter alia in different levels of TPI expression in various tissues.]. 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:8244340
;
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:NP358644.RA97tf_P3SS5Pja183cbw3QvPgdMIep0IyNFzfj6kiuF8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:30+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" .
}