@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU
> .
@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:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_head
{
this:
np:hasAssertion
dgn-np:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_assertion
;
np:hasProvenance
dgn-np:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_provenance
;
np:hasPublicationInfo
dgn-np:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_assertion
a
np:Assertion
.
dgn-np:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_provenance
a
np:Provenance
.
dgn-np:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_assertion
{
miriam-gene:7490
a
ncit:C16612
.
lld:C0004903
a
ncit:C7057
.
dgn-gda:DGN5771cc73872f436e119421e83dfb2fd0
sio:SIO_000628
miriam-gene:7490
,
lld:C0004903
;
a
sio:SIO_001121
.
}
dgn-np:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_provenance
{
dgn-np:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_assertion
dcterms:description
"[Analysis of several somatic cell hybrids containing various derivatives with deletions or translocations revealed that the human MyoD (MYF3) gene is not associated with the WAGR locus at chromosomal band 11p13 nor with the loss of the heterozygosity region at 11p15.5 related to the Beckwith-Wiedemann syndrome.]. 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:2176177
;
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:NP240624.RAoYOeYVfQ3Gepy4sU3P6SGIWXrmDB5_bYSHy5Mq49uFU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}