@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw
> .
@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:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_head
{
this:
np:hasAssertion
dgn-np:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_assertion
;
np:hasProvenance
dgn-np:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_provenance
;
np:hasPublicationInfo
dgn-np:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_assertion
a
np:Assertion
.
dgn-np:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_provenance
a
np:Provenance
.
dgn-np:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_assertion
{
miriam-gene:5244
a
ncit:C16612
.
lld:C0008370
a
ncit:C7057
.
dgn-gda:DGN0f1a9503e4eb54305bc7da3a7911cbc9
sio:SIO_000628
miriam-gene:5244
,
lld:C0008370
;
a
sio:SIO_001121
.
}
dgn-np:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_provenance
{
dgn-np:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_assertion
dcterms:description
"[Defect in ABCB4 function causes the production of bile with low phospholipid content, increased lithogenicity and high detergent properties leading to bile duct luminal membrane injuries and resulting in cholestasis with increased serum gamma-glutamyltransferase (GGT) activity.]. 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:17562004
;
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:NP154230.RAoN47U8fz2fl6EMlqULqVOSlTYISfgvs2xM2Q1RzSTmw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}