@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q
> .
@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:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_head
{
this:
np:hasAssertion
dgn-np:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_assertion
;
np:hasProvenance
dgn-np:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_assertion
a
np:Assertion
.
dgn-np:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_provenance
a
np:Provenance
.
dgn-np:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_assertion
{
miriam-gene:4060
a
ncit:C16612
.
lld:C0271183
a
ncit:C7057
.
dgn-gda:DGN267e66b052392a71ea98c35bad2aa25b
sio:SIO_000628
miriam-gene:4060
,
lld:C0271183
;
a
sio:SIO_001121
.
}
dgn-np:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_provenance
{
dgn-np:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_assertion
dcterms:description
"[Our results indicate that an SNP (rs3759223), which is located in the promoter region of the lumican gene, may be worth further investigation to determine its association with development of high myopia.]. 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:16902402
;
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:NP634263.RAnJur7dYntdqEyQ_LPaqicrF2PrMcZCJ3_FgvDdoXD9Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:22+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" .
}