@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0
> .
@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:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_head
{
this:
np:hasAssertion
dgn-np:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_assertion
;
np:hasProvenance
dgn-np:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_provenance
;
np:hasPublicationInfo
dgn-np:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_assertion
a
np:Assertion
.
dgn-np:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_provenance
a
np:Provenance
.
dgn-np:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_assertion
{
miriam-gene:5226
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGNd1f5cd47cb0877900272462f675b1081
sio:SIO_000628
miriam-gene:5226
,
lld:C0026847
;
a
sio:SIO_001121
.
}
dgn-np:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_provenance
{
dgn-np:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_assertion
dcterms:description
"[Here, for the first time, we report on the heterozygosity analysis of five STR markers (D5S1408, D5S1417, D5S610, D5S629 and D5S637) flanking to SMA gene region, to examine their applicability in the PGD for SMA disease.]. 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:23132709
;
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:NP657493.RA7ZvL13WvfTgxdE_g-Y011dVhWyxqZHN5wRAfU8VB8M0130_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" .
}