@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g
> .
@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:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_head
{
this:
np:hasAssertion
dgn-np:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_assertion
;
np:hasProvenance
dgn-np:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_provenance
;
np:hasPublicationInfo
dgn-np:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_assertion
a
np:Assertion
.
dgn-np:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_provenance
a
np:Provenance
.
dgn-np:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_assertion
{
miriam-gene:5080
a
ncit:C16612
.
lld:C0271183
a
ncit:C7057
.
dgn-gda:DGN882effb9274c84b018573102d7184718
sio:SIO_000628
miriam-gene:5080
,
lld:C0271183
;
a
sio:SIO_001121
.
}
dgn-np:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_provenance
{
dgn-np:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_assertion
dcterms:description
"[The χ(2) test was used to compare the allele and genotype frequencies of SNPs in patients and control subjects and the results showed that ten SNPs of the PAX6, Lumican, and MYOC genes were not significantly associated with 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:22809227
;
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:NP334745.RAMxIR2blgVeeFnAbqo3fBq6fZ7ao4qrj0UdymkMiO6_g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:17+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" .
}