@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk
> .
@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:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_head
{
this:
np:hasAssertion
dgn-np:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion
;
np:hasProvenance
dgn-np:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_provenance
;
np:hasPublicationInfo
dgn-np:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion
a
np:Assertion
.
dgn-np:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_provenance
a
np:Provenance
.
dgn-np:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN888302cf8a8559dd5b57a94bd1dd2bf0
sio:SIO_000628
miriam-gene:4204
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_provenance
{
dgn-np:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_assertion
dcterms:description
"[A number of animal models with complete or partial lack of MeCP2 functions have been generated to correlate the clinical phenotype of Rett syndrome, and studies involving different mutations of MeCP2 have shown similar effects.]. 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:23912219
;
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:NP1099225.RAJlBpBia_E52QmgVw493m_gThGVj8_R1lWjxwkPTOeCk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:04+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: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" .
}