@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM
> .
@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 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:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_head
{
this:
np:hasAssertion
dgn-np:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_assertion
;
np:hasProvenance
dgn-np:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_provenance
;
np:hasPublicationInfo
dgn-np:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_assertion
a
np:Assertion
.
dgn-np:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_provenance
a
np:Provenance
.
dgn-np:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_assertion
{
miriam-gene:21
a
ncit:C16612
.
lld:C0034069
a
ncit:C7057
.
dgn-gda:DGNd84c61206150453c5c6b520dbfec89e6
sio:SIO_000628
miriam-gene:21
,
lld:C0034069
;
a
sio:SIO_001121
.
}
dgn-np:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_provenance
{
dgn-np:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_assertion
dc:description
"[The determination of an ABCA3 mutation in one case of severe pulmonary fibrosis with significant dystrophy of the brain and the identification of four highly similar archival cases and eight others with partial pathological findings supports the designation of an independent disorder, here referred to as the cerebropulmonary dysgenetic syndrome.]. 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:18603241
;
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:NP370177.RADIN46QZRIBIrLYxLs8QBCHigTG0h3JYCo0EWk67p8tM130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:37+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}