@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY
> .
@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:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_head
{
this:
np:hasAssertion
dgn-np:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_assertion
;
np:hasProvenance
dgn-np:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_provenance
;
np:hasPublicationInfo
dgn-np:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_assertion
a
np:Assertion
.
dgn-np:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_provenance
a
np:Provenance
.
dgn-np:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_assertion
{
miriam-gene:4683
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGNa63a27a4332bd6c096f75d02128e99ba
sio:SIO_000628
miriam-gene:4683
,
lld:C0524620
;
a
sio:SIO_001121
.
}
dgn-np:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_provenance
{
dgn-np:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_assertion
dcterms:description
"[The United States CF Foundation recently proposed the term cystic fibrosis transmembrane conductance regulator related metabolic syndrome (CRMS) to describe infants with elevated immunoreactive trypsinogen (IRT) on NBS who do not meet diagnostic criteria for CF.]. 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:21538969
;
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:NP697704.RACzkCnSL72RslE2m9edpZqK0S5XS3StKuY7BCqABUnfY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}