@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs
> .
@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:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_head
{
this:
np:hasAssertion
dgn-np:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_assertion
;
np:hasProvenance
dgn-np:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_provenance
;
np:hasPublicationInfo
dgn-np:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_assertion
a
np:Assertion
.
dgn-np:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_provenance
a
np:Provenance
.
dgn-np:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_assertion
{
miriam-gene:2191
a
ncit:C16612
.
lld:C0751658
a
ncit:C7057
.
dgn-gda:DGNfef94ecbc5f192e41272ed6c01485d6c
sio:SIO_000628
miriam-gene:2191
,
lld:C0751658
;
a
sio:SIO_001121
.
}
dgn-np:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_provenance
{
dgn-np:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_assertion
dcterms:description
"[Although concomitant lesions in the ulnar nerve entrapment site at the wrist cannot be excluded, these findings indicate that CTS is not the sole distinctive feature in the majority of 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:NP614336.RA5YCO4yAyQiN56TSCIqRX6ZHeSVH3qgtnp2imxAZvDBs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:11+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" .
}