@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs
> .
@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:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_head
{
this:
np:hasAssertion
dgn-np:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_assertion
;
np:hasProvenance
dgn-np:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_provenance
;
np:hasPublicationInfo
dgn-np:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_assertion
a
np:Assertion
.
dgn-np:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_provenance
a
np:Provenance
.
dgn-np:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGNe003cdf93eda7374169ac0b8b8a0ea87
sio:SIO_000628
miriam-gene:3342
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_provenance
{
dgn-np:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_assertion
dcterms:description
"[Screening large patient cohorts with mental retardation by array CGH has recently lead to the characterization of many novel microdeletion and microduplication syndromes, initially according to the shared cytogenetic aberrations, with secondary characterization of the corresponding phenotypes.]. 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:18512078
;
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:NP674015.RAN8EyAmJAZm3qMNk_bYaVdnicWLKAd-LWMj_gciMKscs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:50+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
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;
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" .
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pav:version
"v4.0.0" .
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