@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY
> .
@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:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_head
{
this:
np:hasAssertion
dgn-np:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_assertion
;
np:hasProvenance
dgn-np:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_provenance
;
np:hasPublicationInfo
dgn-np:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_assertion
a
np:Assertion
.
dgn-np:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_provenance
a
np:Provenance
.
dgn-np:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_assertion
{
miriam-gene:5046
a
ncit:C16612
.
lld:C0409959
a
ncit:C7057
.
dgn-gda:DGNa76a03b832aba478510eaf1e92b3f8ce
sio:SIO_000628
miriam-gene:5046
,
lld:C0409959
;
a
sio:SIO_001121
.
}
dgn-np:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_provenance
{
dgn-np:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_assertion
dcterms:description
"[These results suggest that a variant in PCSK6 is strongly associated with protection against pain in knee OA, offering some insight as to why, in the presence of the same structural damage, some individuals develop chronic pain and others are protected.]. 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:22440827
;
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:NP564826.RAnoREkGCWY3NKR8Z6iSxhlP0MHYnynQt1vt-aVKsQuKY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}