@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24
> .
@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:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_head
{
this:
np:hasAssertion
dgn-np:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_assertion
;
np:hasProvenance
dgn-np:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_provenance
;
np:hasPublicationInfo
dgn-np:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_assertion
a
np:Assertion
.
dgn-np:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_provenance
a
np:Provenance
.
dgn-np:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_assertion
{
miriam-gene:4671
a
ncit:C16612
.
lld:C0043116
a
ncit:C7057
.
dgn-gda:DGN51957f3d298333f1ad6617d3dcc1e94d
sio:SIO_000628
miriam-gene:4671
,
lld:C0043116
;
a
sio:SIO_001121
.
}
dgn-np:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_provenance
{
dgn-np:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_assertion
dcterms:description
"[The molecular analysis of two marker genes for spinal muscular atrophy (SMA) i.e, the survival motor neuron gene (SMN) and the neuronal apoptosis inhibitory protein gene (NAIP) was conducted in 39 Indian patients with clinical symptoms of SMA.]. 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:16936383
;
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:NP863288.RAPLsqjyIP8zzO3k7r5VdWrIaBjVL1YWQr5JSxV2Pfw24130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:47+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" .
}