@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg
> .
@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:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_head
{
this:
np:hasAssertion
dgn-np:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_assertion
;
np:hasProvenance
dgn-np:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_provenance
;
np:hasPublicationInfo
dgn-np:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_assertion
a
np:Assertion
.
dgn-np:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_provenance
a
np:Provenance
.
dgn-np:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_assertion
{
miriam-gene:196
a
ncit:C16612
.
lld:C0024117
a
ncit:C7057
.
dgn-gda:DGN5f2396354688ad476f0e32a041edb919
sio:SIO_000628
miriam-gene:196
,
lld:C0024117
;
a
sio:SIO_001121
.
}
dgn-np:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_provenance
{
dgn-np:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_assertion
dcterms:description
"[although overlaps exist in the disease characteristics of asthma and COPD, the combination of lung function testing, sputum induction, and AHR reveals information that facilitates the distinction between these diseases, allowing clinicians to better tailor their therapy.]. 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:20856828
;
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:NP913989.RAyg3297MF8eQWj4pqeRZDufQr2MDH7DzXwO9HkD5epwg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:21+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" .
}