@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0
> .
@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:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_head
{
this:
np:hasAssertion
dgn-np:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_assertion
;
np:hasProvenance
dgn-np:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_provenance
;
np:hasPublicationInfo
dgn-np:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_assertion
a
np:Assertion
.
dgn-np:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_provenance
a
np:Provenance
.
dgn-np:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_assertion
{
miriam-gene:6521
a
ncit:C16612
.
lld:C0013902
a
ncit:C7057
.
dgn-gda:DGNf881f4151ff2f7a78986a68e8681a882
sio:SIO_000628
miriam-gene:6521
,
lld:C0013902
;
a
sio:SIO_001121
.
}
dgn-np:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_provenance
{
dgn-np:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_assertion
dcterms:description
"[With the exception of the mutation causing South-East Asian ovalocytosis (SAO), none of these mutations has been reported outside the tropics, where dRTA caused by SLC4A1 mutations is much rarer and almost always dominant, resulting from mutations that are quite different from those found in the tropics.]. 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:22919024
;
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:NP205441.RAg08JpSILZB6izFOmgBpGuZdERuNZHHJrZvp50prtpu0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:53+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" .
}