@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w
> .
@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:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_head
{
this:
np:hasAssertion
dgn-np:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_assertion
;
np:hasProvenance
dgn-np:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_provenance
;
np:hasPublicationInfo
dgn-np:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_assertion
a
np:Assertion
.
dgn-np:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_provenance
a
np:Provenance
.
dgn-np:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_assertion
{
miriam-gene:7050
a
ncit:C16612
.
lld:C0271183
a
ncit:C7057
.
dgn-gda:DGN44937eeb2137c29223368f06fffd4542
sio:SIO_000628
miriam-gene:7050
,
lld:C0271183
;
a
sio:SIO_001121
.
}
dgn-np:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_provenance
{
dgn-np:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_assertion
dcterms:description
"[Four single-nucleotide polymorphisms (SNPs) in the TGIF, lumican, TGFB1, and HGF genes have been declared to be associated with high myopia in Chinese living in southeast China, but none of them has been confirmed by additional studies.]. 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:19060265
;
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:NP156261.RAo3UVSl9XHoF9JtwmtubWU8-GM7TWJFlZPSMudf1xM8w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:24+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" .
}