@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I
> .
@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:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_head
{
this:
np:hasAssertion
dgn-np:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_assertion
;
np:hasProvenance
dgn-np:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_provenance
;
np:hasPublicationInfo
dgn-np:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_assertion
a
np:Assertion
.
dgn-np:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_provenance
a
np:Provenance
.
dgn-np:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0027765
a
ncit:C7057
.
dgn-gda:DGNd32289b70b5017511437c7682e422dfa
sio:SIO_000628
miriam-gene:4204
,
lld:C0027765
;
a
sio:SIO_001122
.
}
dgn-np:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_provenance
{
dgn-np:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_assertion
dcterms:description
"[The many clinical features found in RTT and the various clinical problems that result from alteration in MeCP2 function have led to the belief that understanding RTT will provide insight into a number of other neurological disorders.]. 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:23226951
;
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:NP1034944.RAlqbOMfeVP91wD_-IirhKPI0V7vRr-DpnES-d509k31I130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:35+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" .
}