@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY
> .
@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:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_head
{
this:
np:hasAssertion
dgn-np:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_assertion
;
np:hasProvenance
dgn-np:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_provenance
;
np:hasPublicationInfo
dgn-np:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_assertion
a
np:Assertion
.
dgn-np:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_provenance
a
np:Provenance
.
dgn-np:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN9c121efdd14899f5771a9c0aadb50e32
sio:SIO_000628
miriam-gene:3342
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_provenance
{
dgn-np:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_assertion
dcterms:description
"[Introduction of array-CGH has brought higher sensitivity with automated DNA fragment analyzer and DNA chip for submicroscopic chromosomal anomalies that are missed till date in many of the acquired and constitutional genetic 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:20112804
;
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:NP597939.RApn5jZBSMh3O4O78A5WWxxSW6CkFJ8WfnpaNbymFxwEY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:59+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" .
}