@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g
> .
@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:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_head
{
this:
np:hasAssertion
dgn-np:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_assertion
;
np:hasProvenance
dgn-np:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_provenance
;
np:hasPublicationInfo
dgn-np:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_assertion
a
np:Assertion
.
dgn-np:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_provenance
a
np:Provenance
.
dgn-np:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_assertion
{
miriam-gene:22937
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN1759eecebef05760db5de135d537468f
sio:SIO_000628
miriam-gene:22937
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_provenance
{
dgn-np:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_assertion
dcterms:description
"[Ninety nine patients from the South Carolina autism project (SCAP) were screened for MeCP2 mutations, including all 41 female patients from whom DNA samples were available plus the 58 male patients with the lowest scores on standard IQ tests and/or the Vineland Adaptive Behavior Scale.]. 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:12555243
;
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:NP686293.RAVdQIuhQor751GWcB8wyCNoYnhyE-GJ4ItZUt0Jq9D0g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:57+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" .
}