@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_head
{
this:
np:hasAssertion
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_assertion
;
np:hasProvenance
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_provenance
;
np:hasPublicationInfo
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_assertion
a
np:Assertion
.
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_provenance
a
np:Provenance
.
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_assertion
{
miriam-gene:2539
a
ncit:C16612
.
lld:C0020433
a
ncit:C7057
.
dgn-gda:DGNcb7ce30e8e07c6b1b3d220b561599242
sio:SIO_000628
miriam-gene:2539
,
lld:C0020433
;
a
sio:SIO_001122
.
}
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_provenance
{
dgn-np:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_assertion
dcterms:description
"[It was not possible to assess the influence of abnormal alleles in the severity of the neonatal hyperbilirubinemia. However, these abnormal alleles did not account for the severity of jaundice in children who presented variants related to CNSHA, since 5 w]. 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:12680285
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP51872.RAtnVKLLJFD_xyNIaoKxGikVgZrqs_ovvfm29iGu9fHpk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:08+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}