@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78
> .
@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:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_head
{
this:
np:hasAssertion
dgn-np:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_assertion
;
np:hasProvenance
dgn-np:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_provenance
;
np:hasPublicationInfo
dgn-np:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_assertion
a
np:Assertion
.
dgn-np:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_provenance
a
np:Provenance
.
dgn-np:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_assertion
{
miriam-gene:10058
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN8954e77541314378ae77bbca4535a53b
sio:SIO_000628
miriam-gene:10058
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_provenance
{
dgn-np:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_assertion
dcterms:description
"[The cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel, an ATP binding cassette (ABC) protein whose defects cause the deadly genetic disease cystic fibrosis (CF), encompasses two nucleotide binding domains (NBD1 and NBD2).]. 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:20861014
;
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:NP292567.RAMlFBuh5OWmaq4T9BweyaSY0e4w3uNxYeNdKF277DV78130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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" .
}