@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk
> .
@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:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_head
{
this:
np:hasAssertion
dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_assertion
;
np:hasProvenance
dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_provenance
;
np:hasPublicationInfo
dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_assertion
a
np:Assertion
.
dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_provenance
a
np:Provenance
.
dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_assertion
{
miriam-gene:182
a
ncit:C16612
.
lld:C0015544
a
ncit:C7057
.
dgn-gda:DGNb07236d1b00e3be122725bbeb328bc62
sio:SIO_000628
miriam-gene:182
,
lld:C0015544
;
a
sio:SIO_001121
.
}
dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_provenance
{
dgn-np:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_assertion
dcterms:description
"[Arteriohepatic dysplasia (AHD, Alagille's syndrome) is presumed to be one of the six known familial intrahepatic cholestatic syndromes, all of which present with neonatal jaundice or failure to thrive, or both.]. 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:7254780
;
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:NP173861.RATbZwVQbOJaB2g4lAvcePAjEJQm4O9sP4WlBlRpbWbyk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}