@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g
> .
@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:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_head
{
this:
np:hasAssertion
dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_assertion
;
np:hasProvenance
dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_provenance
;
np:hasPublicationInfo
dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_assertion
a
np:Assertion
.
dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_provenance
a
np:Provenance
.
dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_assertion
{
miriam-gene:51440
a
ncit:C16612
.
lld:C0020443
a
ncit:C7057
.
dgn-gda:DGNe3aaab72c30324de548da00031d7bdd2
sio:SIO_000628
miriam-gene:51440
,
lld:C0020443
;
a
sio:SIO_001121
.
}
dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_provenance
{
dgn-np:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_assertion
dcterms:description
"[By means of mutant allele-specific amplification we determined that the mutation co-segregated with elevated cholesterol and LDL cholesterol in the plasma of family members with HLP IIa and HLP IIb, but not with the elevated plasma triglycerides seen in HLP IIb and HLP IV patients.]. 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:10807540
;
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:NP861515.RAR6AmUlEs0MUdOw1Vt8gyDT0FgNkiwVYbxzIcUwjCv2g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:46+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" .
}