@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc
> .
@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:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_head
{
this:
np:hasAssertion
dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_assertion
;
np:hasProvenance
dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_provenance
;
np:hasPublicationInfo
dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_assertion
a
np:Assertion
.
dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_provenance
a
np:Provenance
.
dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_assertion
{
miriam-gene:338
a
ncit:C16612
.
lld:C0010054
a
ncit:C7057
.
dgn-gda:DGNef589a78beca7776470f303e42d89263
sio:SIO_000628
miriam-gene:338
,
lld:C0010054
;
a
sio:SIO_001121
.
}
dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_provenance
{
dgn-np:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_assertion
dcterms:description
"[The role of genetic variation at the 3' end of the apolipoprotein B gene locus in the development of coronary heart disease and the regulation of the serum levels of various lipoproteins was studied by using two common restriction fragment length polymorphisms detected with the enzymes Xba I and EcoR I.]. 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:1967524
;
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:NP299227.RA_dD5aL_KTk0gw78cibGJpWR7ZKj8EpdZqPQYtW-tbkc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}