@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4
> .
@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:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_head
{
this:
np:hasAssertion
dgn-np:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_assertion
;
np:hasProvenance
dgn-np:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_provenance
;
np:hasPublicationInfo
dgn-np:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_assertion
a
np:Assertion
.
dgn-np:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_provenance
a
np:Provenance
.
dgn-np:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_assertion
{
miriam-gene:5243
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN9e84833745528f7d0616003d6099db68
sio:SIO_000628
miriam-gene:5243
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_provenance
{
dgn-np:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_assertion
dcterms:description
"[Heterologous expression of wild-type or mutated MDR1 revealed similar mRNA transcript levels in Chinese hamster ovary K1 recipients, but the subsequent processing was defective for all mutations that give rise to severe cystic fibrosis in the case of CFTR.]. 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:7914197
;
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:NP615170.RAjtyr_7wiCBa6ZV3HI9QN1_e7hRZRONPb80EBR5P3vs4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:12+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" .
}