@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ
> .
@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:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_head
{
this:
np:hasAssertion
dgn-np:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_assertion
;
np:hasProvenance
dgn-np:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_assertion
a
np:Assertion
.
dgn-np:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_provenance
a
np:Provenance
.
dgn-np:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_assertion
{
miriam-gene:21
a
ncit:C16612
.
lld:C1704437
a
ncit:C7057
.
dgn-gda:DGN6c069df6228b97a733001673490d4bb5
sio:SIO_000628
miriam-gene:21
,
lld:C1704437
;
a
sio:SIO_001121
.
}
dgn-np:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_provenance
{
dgn-np:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_assertion
dcterms:description
"[Term infants carrying the E292V missense mutation of the gene encoding ABCA3 are likely to develop respiratory distress syndrome, and the mutation has also been linked to interstitial lung disease in paediatric patients.]. 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:22145626
;
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:NP647956.RA0QDTtHutzfDVrIltEJxrFiNPAUpzYzKkqFOlg_bPsGQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:30+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" .
}