@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4
> .
@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:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_head
{
this:
np:hasAssertion
dgn-np:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_assertion
;
np:hasProvenance
dgn-np:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_assertion
a
np:Assertion
.
dgn-np:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_provenance
a
np:Provenance
.
dgn-np:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_assertion
{
miriam-gene:3381
a
ncit:C16612
.
lld:C0020433
a
ncit:C7057
.
dgn-gda:DGNe2475e0626b4167cc015e23543e375ea
sio:SIO_000628
miriam-gene:3381
,
lld:C0020433
;
a
sio:SIO_001121
.
}
dgn-np:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_provenance
{
dgn-np:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_assertion
dcterms:description
"[The lower BSP uptake in GS is not secondary to the hyperbilirubinemia, but probably caused by (an) independent, genetically determined defect(s) in hepatic transport mechanism(s), shared by BSP and bilirubin, that are likely necessary for phenotypic expression of GS.]. 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:11230743
;
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:NP581026.RAGUK_Ya26JHJZC1GV1RU9xqNRBHmIZtGLOKiqfILLiJ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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" .
}