@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s
> .
@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:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_head
{
this:
np:hasAssertion
dgn-np:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_assertion
;
np:hasProvenance
dgn-np:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_assertion
a
np:Assertion
.
dgn-np:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_provenance
a
np:Provenance
.
dgn-np:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_assertion
{
miriam-gene:2548
a
ncit:C16612
.
lld:C0002986
a
ncit:C7057
.
dgn-gda:DGN91578af74cdb11760da6ac2dd26d0a14
sio:SIO_000628
miriam-gene:2548
,
lld:C0002986
;
a
sio:SIO_001121
.
}
dgn-np:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_provenance
{
dgn-np:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_assertion
dcterms:description
"[Over the next 13 years, enzyme replacement therapy became clinically available for the treatment of Fabry disease, mucopolysaccharidosis Type I, mucopolysaccharidosis Type II, mucopolysaccharidosis Type VI, and glycogen storage disease Type II.]. 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:18641514
;
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:NP900897.RAH72ghOHEIvlThZa6zshdDd_M-yT9OVgnqLaKkNsb1_s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:13+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" .
}