@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA
> .
@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:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_head
{
this:
np:hasAssertion
dgn-np:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_assertion
;
np:hasProvenance
dgn-np:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_provenance
;
np:hasPublicationInfo
dgn-np:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_assertion
a
np:Assertion
.
dgn-np:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_provenance
a
np:Provenance
.
dgn-np:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0024115
a
ncit:C7057
.
dgn-gda:DGN7fe16e55cc75aae5272c5cb2610df8f1
sio:SIO_000628
miriam-gene:2944
,
lld:C0024115
;
a
sio:SIO_001121
.
}
dgn-np:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_provenance
{
dgn-np:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_assertion
dcterms:description
"[The frequency of the DF508 CFTR mutation, as well as of the GSTM1 and GSTT1 genotypes, was not found to be associated with gender, ethnicity, pulmonary disease status, or pancreatic disease status.]. 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:22407040
;
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:NP757856.RAnuvU4QC5DxU8cX33nQ9xpBjMshyiE11026V5aPJVqCA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:39+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" .
}