@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98
> .
@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:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_head
{
this:
np:hasAssertion
dgn-np:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_assertion
;
np:hasProvenance
dgn-np:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_provenance
;
np:hasPublicationInfo
dgn-np:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_assertion
a
np:Assertion
.
dgn-np:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_provenance
a
np:Provenance
.
dgn-np:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_assertion
{
miriam-gene:6399
a
ncit:C16612
.
lld:C0029422
a
ncit:C7057
.
dgn-gda:DGNd885e515266df5cf151b24d11808fb41
sio:SIO_000628
miriam-gene:6399
,
lld:C0029422
;
a
sio:SIO_001121
.
}
dgn-np:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_provenance
{
dgn-np:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_assertion
dcterms:description
"[The results of our study expand the spectrum of SEDLIN mutations associated with SEDT, and this will help to elucidate further the role of this novel protein in the etiology of this form of osteochondrodysplasia.]. 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:11443194
;
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:NP371033.RA9dM3F0z4snVeMe6S1RSfB2jw7PX41rjrA4cTL-WoA98130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:37+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" .
}