@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo
> .
@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:NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo130_head
{
this:
np:hasAssertion
dgn-np:NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo130_assertion
a
np:Assertion
.
dgn-np:NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo130_provenance
a
np:Provenance
.
dgn-np:NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo130_publicationInfo
a
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.
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dgn-np:NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo130_assertion
{
miriam-gene:79084
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN33bf120f0a8f0fc0da5e008da5070403
sio:SIO_000628
miriam-gene:79084
,
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;
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.
}
dgn-np:NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo130_provenance
{
dgn-np:NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo130_assertion
dcterms:description
"[Our purpose was the determination of a possible genotype-phenotype correlation between the copy number of SMN2, NAIP, p44, H4F5 and occludin genes localized in the same SMN1 region (5q13) and the severity of the disease in SMA Tunisian patients.]. 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:21821450
;
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:NP725068.RA5kQ_VjgkIVhV-qnVlfkE8rNqRk129tKW4wHi1bRtRbo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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
<
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> ;
pav:version
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dgn-void:disgenetrdf
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}