@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI
> .
@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:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_head
{
this:
np:hasAssertion
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_assertion
;
np:hasProvenance
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_provenance
;
np:hasPublicationInfo
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_assertion
a
np:Assertion
.
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_provenance
a
np:Provenance
.
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0024115
a
ncit:C7057
.
dgn-gda:DGNeda7d81477ab62820a8654a5f828edd2
sio:SIO_000628
miriam-gene:1080
,
lld:C0024115
;
a
sio:SIO_001121
.
}
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_provenance
{
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_assertion
dcterms:description
"[Twin and sibling analysis indicates that modifier genes, rather than allelic variation in CFTR, are responsible for most of the variability in severity of lung disease, the major cause of mortality in CF patients.]. 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:18424453
;
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 .
}
dgn-np:NP666818.RAhlXEAHAC6ztKF5-XYVUzWUo8NbHkp-ZWPTp44uJl-sI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:47+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}