@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0
> .
@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:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_head
{
this:
np:hasAssertion
dgn-np:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_assertion
;
np:hasProvenance
dgn-np:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_provenance
;
np:hasPublicationInfo
dgn-np:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_assertion
a
np:Assertion
.
dgn-np:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_provenance
a
np:Provenance
.
dgn-np:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_assertion
{
miriam-gene:4320
a
ncit:C16612
.
lld:C0027092
a
ncit:C7057
.
dgn-gda:DGNb06bf2d9bb2153c807674246736dc422
sio:SIO_000628
miriam-gene:4320
,
lld:C0027092
;
a
sio:SIO_001121
.
}
dgn-np:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_provenance
{
dgn-np:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_assertion
dcterms:description
"[Initial findings indicated that the best p values for each trait were 0.02 for myopia at rs2274755 (MMP9), 0.02 for SE at both rs3740938 (MMP8) and rs131451 (MMP11), 0.01 for axial length at rs11225395 (MMP8), 0.01 for anterior chamber depth at rs498186 (MMP1) and 0.02 at rs10488 (MMP1).]. 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:23077567
;
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:NP871660.RAWjV-u0KgZSueFZJ74s6P4SAbnFwwhuRRvthpo6FfNx0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:53+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" .
}