@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto
> .
@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:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_head
{
this:
np:hasAssertion
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion
;
np:hasProvenance
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance
;
np:hasPublicationInfo
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion
a
np:Assertion
.
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance
a
np:Provenance
.
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion
{
miriam-gene:6439
a
ncit:C16612
.
lld:C0020630
a
ncit:C7057
.
dgn-gda:DGN73a1a91b362721e086854b2d153f5ca8
sio:SIO_000628
miriam-gene:6439
,
lld:C0020630
;
a
sio:SIO_001121
.
}
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_provenance
{
dgn-np:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_assertion
dcterms:description
"[Although the relative abundance of the deletion form of SP-B mRNA remains constant among normal lungs, it is found with relatively higher abundance in the lungs of some individuals with diseases such as congenital alveolar proteinosis, respiratory distress syndrome, bronchopulmonary dysplasia, alveolar capillary dysplasia and hypophosphatasia.]. 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:10493923
;
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:NP591018.RAC1Th0KJ3RFaszDnmjXWEzSUtA__FnydiLnkuco8cCto130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}