@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc
> .
@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:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_head
{
this:
np:hasAssertion
dgn-np:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_assertion
;
np:hasProvenance
dgn-np:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_provenance
;
np:hasPublicationInfo
dgn-np:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_assertion
a
np:Assertion
.
dgn-np:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_provenance
a
np:Provenance
.
dgn-np:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_assertion
{
miriam-gene:6606
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN7d5808bdc9fcaa6c56dfd1abdb6649b5
sio:SIO_000628
miriam-gene:6606
,
lld:C0026847
;
a
sio:SIO_001122
.
}
dgn-np:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_provenance
{
dgn-np:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_assertion
dcterms:description
"[The exon 7 and the flanking area of the SMN1 and SMN2 genes of 55 SMA patients and 46 unrelated normal individuals were amplified with asymmetric PCR with unlabeled probe and symmetric PCR without probe, respectively.]. 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:19480685
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP62005.RAVFFK3HqNLQhDzoSJYNhMEN9FfyFHY0efTo1HW5UDWBc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}