@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo
> .
@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:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_head
{
this:
np:hasAssertion
dgn-np:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_assertion
;
np:hasProvenance
dgn-np:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_provenance
;
np:hasPublicationInfo
dgn-np:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_assertion
a
np:Assertion
.
dgn-np:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_provenance
a
np:Provenance
.
dgn-np:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_assertion
{
miriam-gene:4747
a
ncit:C16612
.
lld:C1862939
a
ncit:C7057
.
dgn-gda:DGN249a9451050a20697638b810b057e110
sio:SIO_000628
miriam-gene:4747
,
lld:C1862939
;
a
sio:SIO_001121
.
}
dgn-np:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_provenance
{
dgn-np:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_assertion
dcterms:description
"[These data suggest that NFL mRNA reductions are common to SALS and FALS patients, and that cells and mice expressing mutant SOD1 may enable us to characterize the molecular mechanism(s) responsible for the loss of neurofilament mRNA.]. 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:12358759
;
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:NP510793.RAqdwISIoDyRWlmj7QPdo1G5YsqBXPa3BLvE3a1HJ6ZPo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}