@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA
> .
@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:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_head
{
this:
np:hasAssertion
dgn-np:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_assertion
;
np:hasProvenance
dgn-np:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_provenance
;
np:hasPublicationInfo
dgn-np:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_assertion
a
np:Assertion
.
dgn-np:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_provenance
a
np:Provenance
.
dgn-np:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_assertion
{
miriam-gene:10599
a
ncit:C16612
.
lld:C0017758
a
ncit:C7057
.
dgn-gda:DGNee89629ba593672e93f1fb1fbdf4f2b2
sio:SIO_000628
miriam-gene:10599
,
lld:C0017758
;
a
sio:SIO_001121
.
}
dgn-np:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_provenance
{
dgn-np:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_assertion
dcterms:description
"[Although glucose-6-phosphate dehydrogenase (G6PD) deficiency is known to be associated with the development of neonatal hyperbilirubinemia, it was observed that in neonates severe hyperbilirubinemia caused by G6PD deficiency, without associated polymorphisms in the UGT1A1 or the OATP2 gene, was preventable.]. 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:15965581
;
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:NP290908.RAr8CvVUYNOM6ZPABcDJUbNZ6USwBnfmBDxdkli5HokxA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:45+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" .
}