@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU
> .
@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:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_head
{
this:
np:hasAssertion
dgn-np:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_assertion
;
np:hasProvenance
dgn-np:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_provenance
;
np:hasPublicationInfo
dgn-np:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_assertion
a
np:Assertion
.
dgn-np:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_provenance
a
np:Provenance
.
dgn-np:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_assertion
{
miriam-gene:4023
a
ncit:C16612
.
lld:C0020480
a
ncit:C7057
.
dgn-gda:DGN16d7c622ffb12b8525005766f9a3b721
sio:SIO_000628
miriam-gene:4023
,
lld:C0020480
;
a
sio:SIO_001121
.
}
dgn-np:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_provenance
{
dgn-np:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_assertion
dcterms:description
"[The purpose of this study was to develop an improved method of direct DNA sequencing, which makes it possible to identify heterozygous mutations of the lipoprotein lipase (LPL) gene in order to understand the underlying genetic disorder of type IV hyperlipoproteinemia.]. 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:9209790
;
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:NP854488.RAArhfM0CpE2BBjX8bIrqQqBLbcd2NQsDDfqouHuCI8iU130_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" .
}