@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU
> .
@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:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_head
{
this:
np:hasAssertion
dgn-np:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_assertion
;
np:hasProvenance
dgn-np:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_provenance
;
np:hasPublicationInfo
dgn-np:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_assertion
a
np:Assertion
.
dgn-np:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_provenance
a
np:Provenance
.
dgn-np:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_assertion
{
miriam-gene:6441
a
ncit:C16612
.
lld:C0035204
a
ncit:C7057
.
dgn-gda:DGN7347257f4b2fa86c336a4889b403425f
sio:SIO_000628
miriam-gene:6441
,
lld:C0035204
;
a
sio:SIO_001121
.
}
dgn-np:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_provenance
{
dgn-np:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_assertion
dcterms:description
"[These results give further insight into the genetic risk factors for complex neonatal respiratory diseases and provide more evidence of the importance of SFTPD and ACE in the etiology of RDS and BPD, respectively.]. 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:21960125
;
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:NP857895.RAJb96p0kxKAKzcEzhD-a5ErXLCg-Odwx5MueeVGWebSU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:44+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" .
}