@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY
> .
@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:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_head
{
this:
np:hasAssertion
dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_assertion
;
np:hasProvenance
dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_provenance
;
np:hasPublicationInfo
dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_assertion
a
np:Assertion
.
dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_provenance
a
np:Provenance
.
dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0023895
a
ncit:C7057
.
dgn-gda:DGN7c49f5100ae42788ac527d1138ab9366
sio:SIO_000628
miriam-gene:1080
,
lld:C0023895
;
a
sio:SIO_001121
.
}
dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_provenance
{
dgn-np:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_assertion
dcterms:description
"[A genotype-phenotype correlation has been observed only with pancreas status, while severity of lung involvement is not clearly related to the CFTR genotype, suggesting that this phenotype might be modulated by additional genetic or environmental factors; liver disease in general is not genetically determined.]. 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:8949420
;
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:NP798834.RAIoCdevp8WMbYCB233DBEjHNPjn3cHnqtLCmdzyA7vuY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}