@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg
> .
@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:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_head
{
this:
np:hasAssertion
dgn-np:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_assertion
;
np:hasProvenance
dgn-np:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_provenance
;
np:hasPublicationInfo
dgn-np:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_assertion
a
np:Assertion
.
dgn-np:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_provenance
a
np:Provenance
.
dgn-np:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_assertion
{
miriam-gene:10683
a
ncit:C16612
.
lld:C0410528
a
ncit:C7057
.
dgn-gda:DGN041edafbeeb7e8bac437e09991630342
sio:SIO_000628
miriam-gene:10683
,
lld:C0410528
;
a
sio:SIO_001121
.
}
dgn-np:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_provenance
{
dgn-np:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_assertion
dcterms:description
"[This study demonstrates that Dll3(neo) and Dll3(pu) are functionally equivalent alleles with respect to the skeletal dysplasia, and we suggest that the three human DLL3 mutations associated with spondylocostal dysplasia are also functionally equivalent to the Dll3(neo) null allele.]. 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:11923214
;
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:NP886791.RA5UxUMOWe44dtk7QWPoy5Jj3qBk63i7nw7FWCH14r_wg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:04+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" .
}