@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I
> .
@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:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_head
{
this:
np:hasAssertion
dgn-np:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_assertion
;
np:hasProvenance
dgn-np:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_provenance
;
np:hasPublicationInfo
dgn-np:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_assertion
a
np:Assertion
.
dgn-np:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_provenance
a
np:Provenance
.
dgn-np:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_assertion
{
miriam-gene:372
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN9b723bc9a7bfe5253dfa1d1c0be217b7
sio:SIO_000628
miriam-gene:372
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_provenance
{
dgn-np:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_assertion
dcterms:description
"[The most frequent causes of missing the diagnosis are (1) atypical clinical presentation, (2) misconceptions about age of onset of childhood asthma, and (3) the coexistence of another chronic respiratory illness that may have a more dramatic clinical picture and constitute a `red herring.` It is fascinating to speculate on the similarities and differences between classical asthma (which has a usually completely reversible obstruction) and the hyperreactivity and partial reversibility of chronic inflammatory diseases like COPD or CF.]. 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:3896051
;
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:NP360130.RAcerc1BB2ecxVcdWpL_UnLtLxsrHFfHzpVpaJCJURW4I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:31+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" .
}