@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg
> .
@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:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_head
{
this:
np:hasAssertion
dgn-np:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_assertion
;
np:hasProvenance
dgn-np:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_provenance
;
np:hasPublicationInfo
dgn-np:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_assertion
a
np:Assertion
.
dgn-np:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_provenance
a
np:Provenance
.
dgn-np:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C1297882
a
ncit:C7057
.
dgn-gda:DGN768155d82c07cd41ffbebd21b0339a61
sio:SIO_000628
miriam-gene:3342
,
lld:C1297882
;
a
sio:SIO_001121
.
}
dgn-np:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_provenance
{
dgn-np:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_assertion
dcterms:description
"[The combination of classical karyotyping, CGH, and FISH is useful for the identification and characterization of partial trisomies in clinical diagnostic laboratories, in order to delineate the chromosome regions implicated in specific clinical 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:11260211
;
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:NP640136.RAnAGI76g92sLIQ_k0nkmmVhMyq0tgExoAiqFMjhR8zZg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:26+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" .
}