@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM
> .
@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:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_head
{
this:
np:hasAssertion
dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_assertion
;
np:hasProvenance
dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_provenance
;
np:hasPublicationInfo
dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_assertion
a
np:Assertion
.
dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_provenance
a
np:Provenance
.
dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_assertion
{
miriam-gene:338
a
ncit:C16612
.
lld:C0020473
a
ncit:C7057
.
dgn-gda:DGNc78d5ca1dfb47aacae409fe53d7a4648
sio:SIO_000628
miriam-gene:338
,
lld:C0020473
;
a
sio:SIO_001122
.
}
dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_provenance
{
dgn-np:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_assertion
dcterms:description
"[We conclude that this arginine 3500 is essential to the function of apoB and that its loss and replacement by glutamine or tryptophan is responsible for the hypercholesterolemia of familial defective apoB 100.]. 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:7627691
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48395.RAIOU1-x9WCkEHGh697wywo0BFtBQWr9R4c544PI_WRtM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}