@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0
> .
@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:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_head
{
this:
np:hasAssertion
dgn-np:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_assertion
;
np:hasProvenance
dgn-np:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_provenance
;
np:hasPublicationInfo
dgn-np:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_assertion
a
np:Assertion
.
dgn-np:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_provenance
a
np:Provenance
.
dgn-np:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_assertion
{
miriam-gene:6337
a
ncit:C16612
.
lld:C0021831
a
ncit:C7057
.
dgn-gda:DGN123b2061012a5d535a5c132728c6090a
sio:SIO_000628
miriam-gene:6337
,
lld:C0021831
;
a
sio:SIO_001121
.
}
dgn-np:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_provenance
{
dgn-np:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_assertion
dcterms:description
"[p.W493R-SCNN1A was detected in three female carriers of F508del CFTR who did not show any symptoms of respiratory or intestinal disease that could be interpreted as the manifestation of CF or CFTR-related disorder.]. 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:21917531
;
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:NP913566.RAI8sIwVEYNa4j4Tliifbqq084lu7AhXmzSeTh2cVpjD0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:20+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" .
}