@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y
> .
@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:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_head
{
this:
np:hasAssertion
dgn-np:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_assertion
;
np:hasProvenance
dgn-np:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_assertion
a
np:Assertion
.
dgn-np:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_provenance
a
np:Provenance
.
dgn-np:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0030286
a
ncit:C7057
.
dgn-gda:DGN2e1aa92479ff7eca3a38892f51cea219
sio:SIO_000628
miriam-gene:1080
,
lld:C0030286
;
a
sio:SIO_001121
.
}
dgn-np:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_provenance
{
dgn-np:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_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:NP186357.RA31IfGptvpufB0wRJTaXewEa2qbCYrgFoGUBXdf8Uc0Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}