@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss
> .
@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:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_head
{
this:
np:hasAssertion
dgn-np:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_assertion
;
np:hasProvenance
dgn-np:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_provenance
;
np:hasPublicationInfo
dgn-np:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_assertion
a
np:Assertion
.
dgn-np:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_provenance
a
np:Provenance
.
dgn-np:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_assertion
{
miriam-gene:6869
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN3d78dbaa4824a8ab1246930b572a0358
sio:SIO_000628
miriam-gene:6869
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_provenance
{
dgn-np:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_assertion
dcterms:description
"[In the present paper, biospecific interaction analysis (BIA) was performed using surface plasmon resonance (SPR) and biosensor technologies to detect the Trp1282Ter mutation (W1282X) of the cystic fibrosis (CF) transmembrane conductance regulator (CFTR) gene.]. 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:11438995
;
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:NP508996.RAFEGv2QT96qdLPlCj63QUmQxHqEOTGZiNbUlywtAP0ss130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:03+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" .
}