@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI
> .
@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:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_head
{
this:
np:hasAssertion
dgn-np:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_assertion
;
np:hasProvenance
dgn-np:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_provenance
;
np:hasPublicationInfo
dgn-np:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_assertion
a
np:Assertion
.
dgn-np:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_provenance
a
np:Provenance
.
dgn-np:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_assertion
{
miriam-gene:1760
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN708a7ac373349124d079ea37bb3e40b4
sio:SIO_000628
miriam-gene:1760
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_provenance
{
dgn-np:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_assertion
dcterms:description
"[By using neuronal progeny derived from human embryonic stem cells carrying the causal DM1 mutation, we have identified an early developmental defect in genes involved in neurite formation and the establishment of neuromuscular connections.]. 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:21458401
;
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:NP317947.RAfO4mz5enNeMRbB6C3d4caCaY3UYtswMra9Cw9BNs9UI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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" .
}