@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_assertion
;
np:hasProvenance
dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_provenance
;
np:hasPublicationInfo
dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_assertion
a
np:Assertion
.
dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_provenance
a
np:Provenance
.
dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_assertion
{
miriam-gene:57679
a
ncit:C16612
.
lld:C0234131
a
ncit:C7057
.
dgn-gda:DGN0904c62c077af9ccc4263fdfb2ee35a8
sio:SIO_000628
miriam-gene:57679
,
lld:C0234131
;
a
sio:SIO_001121
.
}
dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_provenance
{
dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_assertion
dcterms:description
"[These mouse models largely fail to recapitulate hallmarks of motor neuron disease, but the subtle deficits that are observed in behavior and pathology have aided in our understanding of the relationship between alsin and motor dysfunction.]. 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:17955197
;
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 .
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dgn-np:NP195625.RAq69Vp3eGsIGy50gGK7643h2ifGiNQ5PIvaTej9mlFRM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
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pav:version
"v2.1.0" .
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