@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ
> .
@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:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_head
{
this:
np:hasAssertion
dgn-np:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_assertion
;
np:hasProvenance
dgn-np:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_assertion
a
np:Assertion
.
dgn-np:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_provenance
a
np:Provenance
.
dgn-np:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_assertion
{
miriam-gene:361
a
ncit:C16612
.
lld:C0027873
a
ncit:C7057
.
dgn-gda:DGN43f904d8459eaeefeae625dad433b5f9
sio:SIO_000628
miriam-gene:361
,
lld:C0027873
;
a
sio:SIO_001121
.
}
dgn-np:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_provenance
{
dgn-np:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_assertion
dcterms:description
"[Recently, allelic mutations were reported at residue 19 of AQP4 in three cases of NMO, and it was suggested that polymorphisms may influence disease by altering AQP4 supramolecular assembly into orthogonal arrays of particles (OAPs).]. 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:21621278
;
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:NP226122.RAQ4vAiI_AvChhRb3B8kjn2SnIG6atETr_K7OIL2L-9TQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}