@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI130_head
{
this:
np:hasAssertion
dgn-np:NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI130_assertion
a
np:Assertion
.
dgn-np:NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI130_provenance
a
np:Provenance
.
dgn-np:NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNcac1fd23913dcdef5e6c8851dbc72888
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001122
.
}
dgn-np:NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI130_provenance
{
dgn-np:NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI130_assertion
dcterms:description
"[In the present work we examined the stability and cellular processing of the Q141K ABCG2 variant, as well as that of the ΔF142 ABCG2, corresponding to the ΔF508 mutation in the CFTR (ABCC7) protein, causing cystic fibrosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:23800412
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP1088953.RALJ1inCVWNN6U4CneojNPdAO6Lb8um0cKEbdssxG7WYI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:59+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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
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pav:version
"v4.0.0" .
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