@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw
> .
@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:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_head
{
this:
np:hasAssertion
dgn-np:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_assertion
;
np:hasProvenance
dgn-np:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_provenance
;
np:hasPublicationInfo
dgn-np:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_assertion
a
np:Assertion
.
dgn-np:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_provenance
a
np:Provenance
.
dgn-np:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_assertion
{
miriam-gene:3381
a
ncit:C16612
.
lld:C0017551
a
ncit:C7057
.
dgn-gda:DGN5f48c89cfa7c9d68a1cd1e02a92e7ea2
sio:SIO_000628
miriam-gene:3381
,
lld:C0017551
;
a
sio:SIO_001121
.
}
dgn-np:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_provenance
{
dgn-np:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_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:NP247636.RAAk0tjCJV5r2N1UYoEssI2MwSDnHXzrqjq9o-S7x8Suw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}