@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc
> .
@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:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_head
{
this:
np:hasAssertion
dgn-np:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_assertion
;
np:hasProvenance
dgn-np:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_provenance
;
np:hasPublicationInfo
dgn-np:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_assertion
a
np:Assertion
.
dgn-np:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_provenance
a
np:Provenance
.
dgn-np:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_assertion
{
miriam-gene:6005
a
ncit:C16612
.
lld:C1861455
a
ncit:C7057
.
dgn-gda:DGNa16d3dbc66d535f4f67945eb4f3ab394
sio:SIO_000628
miriam-gene:6005
,
lld:C1861455
;
a
sio:SIO_001122
.
}
dgn-np:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_provenance
{
dgn-np:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_assertion
dcterms:description
"[Since half of the expressed RhAG in OHSt most probably corresponds to the mutated form of RhAG, as expected from the OHSt heterozygous status, this dramatic decrease can be therefore related to the loss of function of the Phe65Ser-mutated RhAG monomer.]. 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:22012326
;
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:NP932276.RAiO9ST9P7v9TJM5nzqeZWZ5CMqzf8_EY2qlw8BYuf0cc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:47+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" .
}