@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo
> .
@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:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_head
{
this:
np:hasAssertion
dgn-np:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_assertion
;
np:hasProvenance
dgn-np:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_provenance
;
np:hasPublicationInfo
dgn-np:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_assertion
a
np:Assertion
.
dgn-np:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_provenance
a
np:Provenance
.
dgn-np:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0600260
a
ncit:C7057
.
dgn-gda:DGNe4c61e9c4bf675309a5ecc02b2be8d92
sio:SIO_000628
miriam-gene:1080
,
lld:C0600260
;
a
sio:SIO_001121
.
}
dgn-np:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_provenance
{
dgn-np:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_assertion
dcterms:description
"[In order to identify a possible hereditary predisposition to the development of obstructive pulmonary disease of unknown origin, we have looked for the presence of Cystic Fibrosis Transmembrane Regulator (CFTR) gene mutations in unrelated patients with no signs of 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:7543317
;
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:NP794649.RAs3PnJLsW0rLhPwgV0d3M1sTpGcVomtxdKLnDnwCprDo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}