@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o
> .
@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:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_head
{
this:
np:hasAssertion
dgn-np:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_assertion
;
np:hasProvenance
dgn-np:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_provenance
;
np:hasPublicationInfo
dgn-np:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_assertion
a
np:Assertion
.
dgn-np:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_provenance
a
np:Provenance
.
dgn-np:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_assertion
{
miriam-gene:176
a
ncit:C16612
.
lld:C0158266
a
ncit:C7057
.
dgn-gda:DGN6cfad322c54ef28729d0d5475674bdae
sio:SIO_000628
miriam-gene:176
,
lld:C0158266
;
a
sio:SIO_001121
.
}
dgn-np:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_provenance
{
dgn-np:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_assertion
dcterms:description
"[An association between the aggrecan variable number of tandem repeat (VNTR) polymorphism and the disc degeneration has been previously reported in Finnish men, and smoking had previously been suspected of causing disc degeneration.]. 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:20367118
;
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:NP608724.RAo3l3ghfUC2Tz-CEWYsKYM4uEAWoQ_6rkXN2suRI466o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}