@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0
> .
@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:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_head
{
this:
np:hasAssertion
dgn-np:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_assertion
;
np:hasProvenance
dgn-np:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_provenance
;
np:hasPublicationInfo
dgn-np:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_assertion
a
np:Assertion
.
dgn-np:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_provenance
a
np:Provenance
.
dgn-np:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0235031
a
ncit:C7057
.
dgn-gda:DGN0301ea55f0252cca8a9d7e67dd4d8e27
sio:SIO_000628
miriam-gene:4397
,
lld:C0235031
;
a
sio:SIO_001121
.
}
dgn-np:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_provenance
{
dgn-np:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_assertion
dcterms:description
"[Axon loss contributes to neurological symptoms in disorders as diverse as multiple sclerosis, stroke, traumatic brain and spinal cord injury, peripheral neuropathies and chronic neurodegenerative diseases, but it has been largely neglected in neuroprotective strategies.]. 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:12220882
;
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:NP851970.RAYB_ueHREEpZZkTXVUXsZ0G5wywD3k_xeLYond6aTKE0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:40+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" .
}