@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8
> .
@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:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_head
{
this:
np:hasAssertion
dgn-np:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_assertion
;
np:hasProvenance
dgn-np:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_provenance
;
np:hasPublicationInfo
dgn-np:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_assertion
a
np:Assertion
.
dgn-np:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_provenance
a
np:Provenance
.
dgn-np:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_assertion
{
miriam-gene:8647
a
ncit:C16612
.
lld:C0005411
a
ncit:C7057
.
dgn-gda:DGN39b9ad401435e96b91540629a35180d3
sio:SIO_000628
miriam-gene:8647
,
lld:C0005411
;
a
sio:SIO_001121
.
}
dgn-np:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_provenance
{
dgn-np:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_assertion
dcterms:description
"[RT-PCR analyses of the liver from two patients with PFIC1, one with PFIC2, one with biliary atresia, showed that, compared to normal liver, hepatic expressions of FXR, SHP, CYP7A1, ASBT were decreased at least by 90% in all cholestatic disorders.]. 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:16628629
;
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:NP271942.RAAh10RYCAXUTyC8sKddjBm5GIPkYgL0tKoi2UdNyZqi8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:33+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" .
}