@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA
> .
@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:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_head
{
this:
np:hasAssertion
dgn-np:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_assertion
;
np:hasProvenance
dgn-np:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_provenance
;
np:hasPublicationInfo
dgn-np:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_assertion
a
np:Assertion
.
dgn-np:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_provenance
a
np:Provenance
.
dgn-np:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0025517
a
ncit:C7057
.
dgn-gda:DGNc2e07dd6fab2183fd73afbec2f3dc288
sio:SIO_000628
miriam-gene:1080
,
lld:C0025517
;
a
sio:SIO_001121
.
}
dgn-np:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_provenance
{
dgn-np:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_assertion
dcterms:description
"[Microbial lung infections are the major cause of morbidity and mortality in the hereditary metabolic disorder cystic fibrosis, yet the molecular mechanisms leading from the mutation of cystic fibrosis transmembrane conductance regulator (CFTR) to lung infection are still unclear.]. 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:18376404
;
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:NP329150.RAQu22NhiCb7xzXoTaH-7uvLxrjJYBbOsvQFNMQ3cGklA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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" .
}