@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY
> .
@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:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_head
{
this:
np:hasAssertion
dgn-np:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_assertion
;
np:hasProvenance
dgn-np:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_provenance
;
np:hasPublicationInfo
dgn-np:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_assertion
a
np:Assertion
.
dgn-np:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_provenance
a
np:Provenance
.
dgn-np:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_assertion
{
miriam-gene:4693
a
ncit:C16612
.
lld:C0035344
a
ncit:C7057
.
dgn-gda:DGNa4780a2bd57f4a014d2d073dd4c0b3c8
sio:SIO_000628
miriam-gene:4693
,
lld:C0035344
;
a
sio:SIO_001122
.
}
dgn-np:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_provenance
{
dgn-np:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_assertion
dcterms:description
"[The incidence of the AA genotype of the C597A polymorphism was considerably higher in advanced-stage ROP cases (83.3%) compared to spontaneously regressing ROP cases (0%) and the normal controls (10.4%) (p < 0.0001). For the other genotypes, no significant difference was detected between the controls and ROP cases. In the case of the C110G mutation in the ND gene, no significant differences were detected between the controls and ROP cases, and the majority of subjects had a CC genotype in all three groups.]. 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:12145535
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP53947.RAAY57I2DA1xPmYP-6lIEA3W_wZ2V-7HvR1u_xhoKVoGY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}