@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg
> .
@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:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_head
{
this:
np:hasAssertion
dgn-np:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_assertion
;
np:hasProvenance
dgn-np:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_provenance
;
np:hasPublicationInfo
dgn-np:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_assertion
a
np:Assertion
.
dgn-np:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_provenance
a
np:Provenance
.
dgn-np:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_assertion
{
miriam-gene:4018
a
ncit:C16612
.
lld:C0020445
a
ncit:C7057
.
dgn-gda:DGN3f193f80d396f3cb5e8d5e7e7735affd
sio:SIO_000628
miriam-gene:4018
,
lld:C0020445
;
a
sio:SIO_001121
.
}
dgn-np:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_provenance
{
dgn-np:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_assertion
dcterms:description
"[Determination of apolipoprotein(a) (apo(a)) phenotype and lipoprotein(a) (Lp(a)) concentration in plasma revealed that in many instances, involving individuals with various apo(a) phenotypes, there was no difference in plasma Lp(a) concentration between an FH heterozygote and an unaffected sibling with the same apo(a) phenotype.]. 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:1830890
;
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:NP421336.RAM_jfkeCPS0-vlPDAIQcnds3eSJX9xvIl2rlLs1vb2Wg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+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" .
}