@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q
> .
@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:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_head
{
this:
np:hasAssertion
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_assertion
;
np:hasProvenance
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_assertion
a
np:Assertion
.
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_provenance
a
np:Provenance
.
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0006267
a
ncit:C7057
.
dgn-gda:DGN76d87ca4a4890dffc1052a5e0d403fec
sio:SIO_000628
miriam-gene:1080
,
lld:C0006267
;
a
sio:SIO_001121
.
}
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_provenance
{
dgn-np:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_assertion
dcterms:description
"[The number of requests is growing, owing to the increasingly wide range of recognized CFTR gene diseases (cystic fibrosis, congenital bilateral absence of the vas deferens, disseminated bronchiectasis, allergic bronchopulmonary aspergillosis and chronic pancreatitis), and the availability of efficient molecular tools for detecting mutations.]. 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:10649490
;
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:NP339108.RA6eQpr2QVAlpdZRKag97atUILwdpcHA74Q5Lv1TBn5_Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}