@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls
> .
@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:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_head
{
this:
np:hasAssertion
dgn-np:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_assertion
;
np:hasProvenance
dgn-np:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_provenance
;
np:hasPublicationInfo
dgn-np:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_assertion
a
np:Assertion
.
dgn-np:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_provenance
a
np:Provenance
.
dgn-np:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_assertion
{
miriam-gene:390226
a
ncit:C16612
.
lld:C0017205
a
ncit:C7057
.
dgn-gda:DGNbb9dc1b6dc770a414cbe37ec4dc45d4e
sio:SIO_000628
miriam-gene:390226
,
lld:C0017205
;
a
sio:SIO_001121
.
}
dgn-np:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_provenance
{
dgn-np:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_assertion
dcterms:description
"[As complex glycans in mammalian cells do not terminate in mannose residues, which are essential for the biological uptake of GCD via macrophage mannose receptors in human patients with Gaucher's disease, an in vitro glycan modification is required in order to expose the mannose residues on the glycans of Cerezyme.]. 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:17524049
;
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:NP389736.RAJyQwykapShSOTTqVeXANreNIm36Q8CjvEDBx3hin0ls130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}