@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI
> .
@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:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_head
{
this:
np:hasAssertion
dgn-np:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_assertion
;
np:hasProvenance
dgn-np:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_provenance
;
np:hasPublicationInfo
dgn-np:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_assertion
a
np:Assertion
.
dgn-np:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_provenance
a
np:Provenance
.
dgn-np:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_assertion
{
miriam-gene:6869
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN2ec860c2ba41a76db1080f671e3b673f
sio:SIO_000628
miriam-gene:6869
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_provenance
{
dgn-np:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_assertion
dcterms:description
"[In the present paper, we applied surface plasmon resonance (SPR) and biosensor technologies for biospecific interaction analysis (BIA) to detect deltaF508 mutation (F508del) of the cystic fibrosis transmembrane regulator (CFTR) gene in both homozygous as well as heterozygous human subjects.]. 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:10338094
;
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:NP589622.RAKbq9t6Qt-n4suXvbpn9ZH6T3kFtiwAba_cAGeUWunvI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}