@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw
> .
@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:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_head
{
this:
np:hasAssertion
dgn-np:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_assertion
;
np:hasProvenance
dgn-np:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_provenance
;
np:hasPublicationInfo
dgn-np:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_assertion
a
np:Assertion
.
dgn-np:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_provenance
a
np:Provenance
.
dgn-np:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_assertion
{
miriam-gene:1418
a
ncit:C16612
.
lld:C0086543
a
ncit:C7057
.
dgn-gda:DGN2a633700f1c8de57ead9d4927287189f
sio:SIO_000628
miriam-gene:1418
,
lld:C0086543
;
a
sio:SIO_001121
.
}
dgn-np:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_provenance
{
dgn-np:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_assertion
dcterms:description
"[This study establishes baseline frequency data for four SNPs in CRYGA and CRYGB genes for future case control studies on the role of these SNPs in the genetic basis of cataract.]. 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:19384013
;
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:NP727719.RA_MuncFiW5d3l2Zh22_TOiZ_XB_WjfFJ_ybZDes2VSfw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:21+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" .
}