@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es
> .
@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:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_head
{
this:
np:hasAssertion
dgn-np:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_assertion
;
np:hasProvenance
dgn-np:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_provenance
;
np:hasPublicationInfo
dgn-np:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_assertion
a
np:Assertion
.
dgn-np:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_provenance
a
np:Provenance
.
dgn-np:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_assertion
{
miriam-gene:6647
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGN2cc66f5d7feb4a61a7b0f98f94df996c
sio:SIO_000628
miriam-gene:6647
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_provenance
{
dgn-np:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_assertion
dcterms:description
"[Literature findings on astrogliosis of the spinal cord and of the cortex of sporadic (SALS) and familial (FALS) cases of amyotrophic lateral sclerosis (ALS) and of SOD1 transgenic mice are analysed and compared with those of 50 autopsied personal cases of ALS.]. 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:15204020
;
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:NP262469.RAInHM7sZ7cNQ7ekhRle4JFDLmF-dfiiPNaPIkJ6cg4Es130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}