@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig
> .
@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:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_head
{
this:
np:hasAssertion
dgn-np:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_assertion
;
np:hasProvenance
dgn-np:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_provenance
;
np:hasPublicationInfo
dgn-np:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_assertion
a
np:Assertion
.
dgn-np:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_provenance
a
np:Provenance
.
dgn-np:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGNbb1364985140b98c33b439ccfc25757a
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_provenance
{
dgn-np:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_assertion
dcterms:description
"[Striking discordance in the phenotype was observed in two pairs of sibs, one of them dizygotic twins, suggesting that factors, genetic and environmental, other than CFTR genotype are important in determining CF phenotype.]. 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:8933333
;
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:NP159366.RASPrjv2W7NE8GeR8228Uzn09NxlurdS6ZsJBb9fQ6Aig130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}