@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ
> .
@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:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_head
{
this:
np:hasAssertion
dgn-np:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_assertion
;
np:hasProvenance
dgn-np:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_assertion
a
np:Assertion
.
dgn-np:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_provenance
a
np:Provenance
.
dgn-np:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_assertion
{
miriam-gene:7276
a
ncit:C16612
.
lld:C0007286
a
ncit:C7057
.
dgn-gda:DGN6a407a60495f4fea83fa6faa137b653e
sio:SIO_000628
miriam-gene:7276
,
lld:C0007286
;
a
sio:SIO_001121
.
}
dgn-np:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_provenance
{
dgn-np:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_assertion
dcterms:description
"[In age-matched idiopathic patients with CTS (20 patients, 27 hands), the slowing of SCV and the prolongation of DML in the median nerve were significant, while the slowing of motor conduction velocity was much less compared to FAP ATTR Val30Met patients.]. 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:19626479
;
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:NP282039.RAG7aoAWm84LkX6-BznaWxaxX5NPLezWNg3iokFVlTtzQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}