@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo
> .
@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:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_head
{
this:
np:hasAssertion
dgn-np:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_assertion
;
np:hasProvenance
dgn-np:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_provenance
;
np:hasPublicationInfo
dgn-np:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_assertion
a
np:Assertion
.
dgn-np:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_provenance
a
np:Provenance
.
dgn-np:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_assertion
{
miriam-gene:3316
a
ncit:C16612
.
lld:C0235025
a
ncit:C7057
.
dgn-gda:DGN204b1dfaf90cc2b9178769a6e043c8fa
sio:SIO_000628
miriam-gene:3316
,
lld:C0235025
;
a
sio:SIO_001121
.
}
dgn-np:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_provenance
{
dgn-np:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_assertion
dcterms:description
"[Thus, it has been demonstrated that mutation of either Hsp27 or the related protein hsp22 can be observed in specific families with hereditary motor neuropathy caused by premature axonal loss, possibly due to neuronal death and subsequent degeneration.]. 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:16048837
;
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:NP750742.RAQF-HpBj0XaH55ff6o28GzDdUObD9TRJEIydG-kSEvbo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:35+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" .
}