@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs
> .
@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:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_head
{
this:
np:hasAssertion
dgn-np:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_assertion
;
np:hasProvenance
dgn-np:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_provenance
;
np:hasPublicationInfo
dgn-np:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_assertion
a
np:Assertion
.
dgn-np:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_provenance
a
np:Provenance
.
dgn-np:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0155877
a
ncit:C7057
.
dgn-gda:DGN5747f2446b146ec6461a584bc74faee0
sio:SIO_000628
miriam-gene:1080
,
lld:C0155877
;
a
sio:SIO_001121
.
}
dgn-np:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_provenance
{
dgn-np:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_assertion
dcterms:description
"[The presence of CFTR mutations was also investigated in 43 white subjects with allergic asthma who did not show sensitization to Aspergillus fumigatus and in 142 subjects seeking genetic counseling for diseases other than cystic fibrosis (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:11243954
;
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:NP225941.RAB1OcjHujukmu8ZcbNu-nFUUAPcUr4356pJTPl4dVXQs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}