@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_head
{
this:
np:hasAssertion
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_assertion
;
np:hasProvenance
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_provenance
;
np:hasPublicationInfo
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_assertion
a
np:Assertion
.
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_provenance
a
np:Provenance
.
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_assertion
{
miriam-gene:7035
a
ncit:C16612
.
lld:C0175693
a
ncit:C7057
.
dgn-gda:DGNbb1461b20cf8af9b66ebb5eb2d1c88f1
sio:SIO_000628
miriam-gene:7035
,
lld:C0175693
;
a
sio:SIO_001121
.
}
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_provenance
{
dgn-np:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_assertion
dcterms:description
"[It is likely that the extent of overall (epi)genetic aberrations exceeded the threshold level for the development of SRS phenotype, but not for the occurrence of other imprinting disorders or recessive Mendelian disorders.]. 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:20685670
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP830718.RAon7QHzXsg6botVovA-yi-pHsJTtZOzB8nYhbV42yVi0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:01+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}