@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o
> .
@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:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_head
{
this:
np:hasAssertion
dgn-np:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_assertion
;
np:hasProvenance
dgn-np:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_provenance
;
np:hasPublicationInfo
dgn-np:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_assertion
a
np:Assertion
.
dgn-np:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_provenance
a
np:Provenance
.
dgn-np:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_assertion
{
miriam-gene:8647
a
ncit:C16612
.
lld:C0085605
a
ncit:C7057
.
dgn-gda:DGN669ef01212be2f71297a6506f4731b47
sio:SIO_000628
miriam-gene:8647
,
lld:C0085605
;
a
sio:SIO_001121
.
}
dgn-np:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_provenance
{
dgn-np:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_assertion
dcterms:description
"[High serum alanine aminotransferase and alphafetoprotein levels, severe lobular lesions with giant hepatocytes, early liver failure, cholelithiasis, hepatocellular carcinoma, very low biliary bile acid concentration, and negative BSEP canalicular staining suggest PFIC2, whereas an absence of these signs and/or presence of extrahepatic manifestations suggest PFIC1.]. 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:20232290
;
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:NP705804.RAmCV-8WUGotC951VgnHk5gzIyE761ojDWuuCkHf4R55o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:09+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
<
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> , <
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" .
}