@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc
> .
@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:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_head
{
this:
np:hasAssertion
dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_assertion
;
np:hasProvenance
dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_provenance
;
np:hasPublicationInfo
dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_assertion
a
np:Assertion
.
dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_provenance
a
np:Provenance
.
dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN2a814465cf8980d05a0239616bf70bb8
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_provenance
{
dgn-np:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_assertion
dcterms:description
"[Genotype-phenotype correlations in cystic fibrosis (CF) may be difficult to establish because of phenotype variability, which is associated with certain CF transmembrane conductance regulator (CFTR) gene mutations and the existence of complex alleles.]. 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:22678879
;
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:NP988278.RAaPbC5FRnNYV5oW82tJgqQut6WK85Smt8HMO4mVm0pAc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:13+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" .
}