@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU
> .
@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:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_head
{
this:
np:hasAssertion
dgn-np:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_assertion
;
np:hasProvenance
dgn-np:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_provenance
;
np:hasPublicationInfo
dgn-np:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_assertion
a
np:Assertion
.
dgn-np:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_provenance
a
np:Provenance
.
dgn-np:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_assertion
{
miriam-gene:1368
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN5f41905a85a4b2287a3806d6cbe12429
sio:SIO_000628
miriam-gene:1368
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_provenance
{
dgn-np:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_assertion
dcterms:description
"[This is the second example of congenital abnormality associated with confined placental mosaicism (CPM) for trisomy 16, without evidence of either UPD or an apparent contribution of abnormal cells to the fetus.]. 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:9267904
;
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:NP686423.RAYeXasc8pkjQQHixpgMbbaD1cMSoOC8XuCcjQjbZY5AU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}