@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o
> .
@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:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_head
{
this:
np:hasAssertion
dgn-np:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_assertion
;
np:hasProvenance
dgn-np:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_provenance
;
np:hasPublicationInfo
dgn-np:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_assertion
a
np:Assertion
.
dgn-np:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_provenance
a
np:Provenance
.
dgn-np:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0263214
a
ncit:C7057
.
dgn-gda:DGN7ea990ba65568926bc73019e475802c5
sio:SIO_000628
miriam-gene:4204
,
lld:C0263214
;
a
sio:SIO_001121
.
}
dgn-np:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_provenance
{
dgn-np:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_assertion
dcterms:description
"[Our results confirm the presence of mutational hot spots in MECP2, broaden the spectrum of mutations, pinpoint additional mutational hot spots and establish that the preserved speech variant is indeed allelic of the classic form.]. 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:10854091
;
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:NP940013.RAcr5eKzvpJfbeMw3y709gRsDwrE7ULIGNwHAccCfzC_o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:36+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" .
}