@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg
> .
@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:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_head
{
this:
np:hasAssertion
dgn-np:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_assertion
;
np:hasProvenance
dgn-np:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_provenance
;
np:hasPublicationInfo
dgn-np:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_assertion
a
np:Assertion
.
dgn-np:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_provenance
a
np:Provenance
.
dgn-np:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_assertion
{
miriam-gene:2717
a
ncit:C16612
.
lld:C0015230
a
ncit:C7057
.
dgn-gda:DGNbfe15aa96e404d6ee25cb10488ad39e2
sio:SIO_000628
miriam-gene:2717
,
lld:C0015230
;
a
sio:SIO_001121
.
}
dgn-np:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_provenance
{
dgn-np:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_assertion
dcterms:description
"[Plasma and leukocyte α-Gal activities were assayed in unrelated healthy young adults of both sexes, who had been genotyped for GLA exon 1, and enzyme activity values in carriers of any of the polymorphisms were compared to those of individuals with the standard genotype; GLA exon 1 was genotyped in males who had α-Gal activity in dried blood spots lower than 2 SD below the cohort average.]. 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:18979223
;
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:NP641345.RATHKC2RlWFtZE14qHvpFJXWFZ_NHV5n9WhVK2GFtEUcg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}