@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE
> .
@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:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_head
{
this:
np:hasAssertion
dgn-np:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_assertion
;
np:hasProvenance
dgn-np:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_provenance
;
np:hasPublicationInfo
dgn-np:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_assertion
a
np:Assertion
.
dgn-np:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_provenance
a
np:Provenance
.
dgn-np:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_assertion
{
miriam-gene:2706
a
ncit:C16612
.
lld:C1961835
a
ncit:C7057
.
dgn-gda:DGN50876cdf40cbf6ebb1d7a4435c7d6b0a
sio:SIO_000628
miriam-gene:2706
,
lld:C1961835
;
a
sio:SIO_001121
.
}
dgn-np:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_provenance
{
dgn-np:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_assertion
dcterms:description
"[The tests included two diseases associated with death in childhood (Niemann-Pick type A and Tay-Sachs disease), five with moderate disability and a variably shortened life span (Bloom syndrome, Canavan disease, cystic fibrosis, familial dysautonomia, Fanconi anemia, and mucolipidosis type IV), and two diseases that are not necessarily disabling or routinely shorten the lifespan (Gaucher disease type I and DFNB1 sensorineural hearing loss).]. 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:15775754
;
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:NP323659.RA91wD_fDMFy43TqNFeMnZ0M8cE4GqPt_cH8fbVnmMWWE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}