@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM
> .
@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:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_head
{
this:
np:hasAssertion
dgn-np:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_assertion
;
np:hasProvenance
dgn-np:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_provenance
;
np:hasPublicationInfo
dgn-np:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_assertion
a
np:Assertion
.
dgn-np:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_provenance
a
np:Provenance
.
dgn-np:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_assertion
{
miriam-gene:8560
a
ncit:C16612
.
lld:C1261287
a
ncit:C7057
.
dgn-gda:DGN10343568d8f80cb8efa3a2d3a5cdec6e
sio:SIO_000628
miriam-gene:8560
,
lld:C1261287
;
a
sio:SIO_001121
.
}
dgn-np:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_provenance
{
dgn-np:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_assertion
dcterms:description
"[Overall, there was no statistically association between the Asn291Ser and Ser447Ter mutations and the baseline or final mean plasma levels of lipids, number of coronary lesions, total occlusions, the mean minimal lumen diameter (MLD) stenoses and the clinical events rate.]. 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:10407505
;
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:NP878803.RAKEKj7_Qmp3aayzb10L79fwDJWLwbfhV641UeW_x3yKM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:57+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" .
}