@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_head
{
this:
np:hasAssertion
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_assertion
;
np:hasProvenance
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_provenance
;
np:hasPublicationInfo
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_assertion
a
np:Assertion
.
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_provenance
a
np:Provenance
.
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_assertion
{
miriam-gene:3931
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGNf0575ec1cbcf00874ca08130090cbf34
sio:SIO_000628
miriam-gene:3931
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_provenance
{
dgn-np:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_assertion
dcterms:description
"[To examine the recent advances in our knowledge of HDL metabolism, composition, function, and coronary heart disease (CHD), as well as marked HDL deficiency states because of mutations in the apolipoprotein (apo) A-I, ATP-binding cassette transfer protein A1 and lecithin cholesterol acyltransferase (LCAT) gene loci.]. 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:24785961
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP532298.RAnCR63jRM9_VeVWLfatmYdBufnL9D0IgnhDVOgUZsbaI130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:54+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}