@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ
> .
@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:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_head
{
this:
np:hasAssertion
dgn-np:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_assertion
;
np:hasProvenance
dgn-np:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_assertion
a
np:Assertion
.
dgn-np:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_provenance
a
np:Provenance
.
dgn-np:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_assertion
{
miriam-gene:2078
a
ncit:C16612
.
lld:C0242225
a
ncit:C7057
.
dgn-gda:DGN6920510f96eace4439eb2f24ab16e35d
sio:SIO_000628
miriam-gene:2078
,
lld:C0242225
;
a
sio:SIO_001121
.
}
dgn-np:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_provenance
{
dgn-np:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_assertion
dcterms:description
"[These results demonstrate the utility of ERG measurements in studies of molecular genetics of color vision deficiencies, and further support the conclusion that not all genes are expressed in color deficient subjects.]. 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:9893852
;
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:NP601228.RAFMo0dvBirGrJg7vd-2Tc6oLYx7m-uRp19MHV8HwOWLQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}