@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8
> .
@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:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_head
{
this:
np:hasAssertion
dgn-np:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_assertion
;
np:hasProvenance
dgn-np:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_provenance
;
np:hasPublicationInfo
dgn-np:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_assertion
a
np:Assertion
.
dgn-np:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_provenance
a
np:Provenance
.
dgn-np:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_assertion
{
miriam-gene:64221
a
ncit:C16612
.
lld:C0700208
a
ncit:C7057
.
dgn-gda:DGNe2c541df4affff4135daa3ab20a3da18
sio:SIO_000628
miriam-gene:64221
,
lld:C0700208
;
a
sio:SIO_001121
.
}
dgn-np:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_provenance
{
dgn-np:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_assertion
dcterms:description
"[More comprehensive examinations of parents and siblings of HGPPS patients are required to determine if the incidence of scoliosis in individuals harbouring heterozygous ROBO3 mutations is greater than in the general population.]. 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:16525029
;
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:NP727889.RAhXglKnrp-rpUapN6RH5WTRWaLfN5FBnuZyOEb4oYAb8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:22+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" .
}