@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_head
{
this:
np:hasAssertion
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_assertion
;
np:hasProvenance
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_assertion
a
np:Assertion
.
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_provenance
a
np:Provenance
.
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN155a3e2e39213a51b4756499aff369cb
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_provenance
{
dgn-np:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_assertion
dcterms:description
"[The spectrum of cystic fibrosis (CF) mutations was determined in 105 patients by using denaturing gradient gel electrophoresis to screen the entire coding regions and adjacent cystic fibrosis transmembrane conductance regulator (CFTR) gene sequences.]. 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:1379210
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP412499.RAzrXF37LFyxvLEsOAR_q69AaP74tI1E_FK3eo_2d4p0Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:52+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}