@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q
> .
@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:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_head
{
this:
np:hasAssertion
dgn-np:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_assertion
;
np:hasProvenance
dgn-np:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_assertion
a
np:Assertion
.
dgn-np:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_provenance
a
np:Provenance
.
dgn-np:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN750675b83e60d76113564a7637bbab7b
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_provenance
{
dgn-np:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_assertion
dcterms:description
"[The disease cystic fibrosis is caused by mutations in CFTR, which can result in defective protein production, defective processing and degradation in the endoplasmic reticulum, or defective channel pore properties or gating properties.]. 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:9759549
;
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:NP1405005.RAGOrtCNYH20lBLSxlz9J01nRHQ8u_IdwOceaKHRXPY8Q130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:23+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" .
}