@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc
> .
@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:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_head
{
this:
np:hasAssertion
dgn-np:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_assertion
;
np:hasProvenance
dgn-np:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_provenance
;
np:hasPublicationInfo
dgn-np:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_assertion
a
np:Assertion
.
dgn-np:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_provenance
a
np:Provenance
.
dgn-np:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_assertion
{
miriam-gene:342977
a
ncit:C16612
.
lld:C0002986
a
ncit:C7057
.
dgn-gda:DGN24238d47f44d7e3f657f6eedf6f57f58
sio:SIO_000628
miriam-gene:342977
,
lld:C0002986
;
a
sio:SIO_001121
.
}
dgn-np:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_provenance
{
dgn-np:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_assertion
dcterms:description
"[While no correlation was found between the GLA genotype and LPWT, the difference of 2.44 mm between the relative LPWT mean values of the two extreme NOS3 groups corresponds to the absolute LPWT increase that an average male patient with Fabry disease experiences during about 12 years.]. 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:18941922
;
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:NP219835.RA8YusKDHos6lEJzvGAgCsqsIQe8d4YToCiIipyzeqIVc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}