@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_head
{
this:
np:hasAssertion
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_assertion
;
np:hasProvenance
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_provenance
;
np:hasPublicationInfo
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_assertion
a
np:Assertion
.
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_provenance
a
np:Provenance
.
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_assertion
{
miriam-gene:5080
a
ncit:C16612
.
lld:C0028738
a
ncit:C7057
.
dgn-gda:DGN468988295aff8f82721983d467fc50e4
sio:SIO_000628
miriam-gene:5080
,
lld:C0028738
;
a
sio:SIO_001121
.
}
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_provenance
{
dgn-np:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_assertion
dcterms:description
"[Analysis of specific diseases, such as albinism and achromatopsia as well as known genetic abnormalities, such as FRMD7 and PAX6 mutations, shows subtle but significant differences between nystagmus subtypes using eye movement recordings.]. 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:21951007
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP926712.RA8yxqWoHSB2b0QwLEZ0nbauCbVmH7tU84bRBV674nBaY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:45+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}