@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno
> .
@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:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_head
{
this:
np:hasAssertion
dgn-np:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_assertion
;
np:hasProvenance
dgn-np:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_provenance
;
np:hasPublicationInfo
dgn-np:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_assertion
a
np:Assertion
.
dgn-np:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_provenance
a
np:Provenance
.
dgn-np:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_assertion
{
miriam-gene:24
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNea3f0a9b95fc095dca64c72a3234809a
sio:SIO_000628
miriam-gene:24
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_provenance
{
dgn-np:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_assertion
dcterms:description
"[Members of the ATP-binding cassette transporter superfamily such as the P-glycoproteins (MDR) and the cystic fibrosis transmembrane conductance regulator (CFTR) share conserved sequence motifs in their nucleotide binding fold that are the major targets for CFTR mutations in patients with cystic fibrosis.]. 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:NP456446.RAQO92KzmkhQHUE7cwtZOylQrYqfvMwRwwChySteD4nno130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:32+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" .
}