@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y
> .
@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:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_head
{
this:
np:hasAssertion
dgn-np:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_assertion
;
np:hasProvenance
dgn-np:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_assertion
a
np:Assertion
.
dgn-np:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_provenance
a
np:Provenance
.
dgn-np:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_assertion
{
miriam-gene:5053
a
ncit:C16612
.
lld:C0024408
a
ncit:C7057
.
dgn-gda:DGN1c4b6da7bb309fb092f30d9379a4f0fc
sio:SIO_000628
miriam-gene:5053
,
lld:C0024408
;
a
sio:SIO_001121
.
}
dgn-np:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_provenance
{
dgn-np:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_assertion
dcterms:description
"[The exclusion of linkage 15 cM on each side of PAH in 16 families with MJD shows that these two forms of dominant ataxia are genetically distinct and at different chromosomal locations (nonallelic).]. 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:7902323
;
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:NP658431.RA5yVSK5QqYpOija7CMU87VI4EOj3a2U7tw7zQRw7tx4Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:36+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" .
}