@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y
> .
@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:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_head
{
this:
np:hasAssertion
dgn-np:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_assertion
;
np:hasProvenance
dgn-np:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_assertion
a
np:Assertion
.
dgn-np:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_provenance
a
np:Provenance
.
dgn-np:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_assertion
{
miriam-gene:6792
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN63aa516a7eaeeae9d563504936abb72e
sio:SIO_000628
miriam-gene:6792
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_provenance
{
dgn-np:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_assertion
dcterms:description
"[The systematic screening of Rett syndrome (RTT) patients for pathogenetic sequence variations has focused on three genes that have been associated with RTT or related clinical phenotypes, namely MECP2, CDKL5, and FOXG1.]. 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:22383159
;
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:NP964799.RARGlz66Z7zdPctvR3msrx0RpGR9Q3Tf4cC0pa7Zxrw4Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:02+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:disgenetv3.0rdf
;
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" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}