@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc
> .
@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:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_head
{
this:
np:hasAssertion
dgn-np:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_assertion
;
np:hasProvenance
dgn-np:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_provenance
;
np:hasPublicationInfo
dgn-np:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_assertion
a
np:Assertion
.
dgn-np:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_provenance
a
np:Provenance
.
dgn-np:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_assertion
{
miriam-gene:2078
a
ncit:C16612
.
lld:C0034951
a
ncit:C7057
.
dgn-gda:DGN4c3e4c654062305b1ad9349383bb1a30
sio:SIO_000628
miriam-gene:2078
,
lld:C0034951
;
a
sio:SIO_001121
.
}
dgn-np:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_provenance
{
dgn-np:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_assertion
dcterms:description
"[Each of these measures was then regressed on age, refractive error (for the ERG), and domain (intradiscal, transmembrane, or cytoplasmic) or codon number of the opsin molecule altered by the mutation.]. 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:7635666
;
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:NP696645.RAptk7Ha-yyZWzZDaBgonwQ28XCBF1r-VsmZclsbWp7lc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}