@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_head
{
this:
np:hasAssertion
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_assertion
;
np:hasProvenance
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_assertion
a
np:Assertion
.
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_provenance
a
np:Provenance
.
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_assertion
{
miriam-gene:4671
a
ncit:C16612
.
lld:C0026847
a
ncit:C7057
.
dgn-gda:DGN8cfb17007b1a2273e3d6cbffdb848854
sio:SIO_000628
miriam-gene:4671
,
lld:C0026847
;
a
sio:SIO_001121
.
}
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_provenance
{
dgn-np:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_assertion
dcterms:description
"[It has been proposed that homozygous loss of SMNT is the primary cause of spinal muscular atrophy while the loss of NAIP and perhaps other genes primarily affects the severity of disease manifestation.]. 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:9225684
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1376938.RAQ7Mw7eDgWUIKAUW9_88N3mJRNsnsXEj90Ms7orrxBqk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:10+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}