@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0
> .
@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:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_head
{
this:
np:hasAssertion
dgn-np:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_assertion
;
np:hasProvenance
dgn-np:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_provenance
;
np:hasPublicationInfo
dgn-np:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_assertion
a
np:Assertion
.
dgn-np:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_provenance
a
np:Provenance
.
dgn-np:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0235820
a
ncit:C7057
.
dgn-gda:DGN88c6da2485983248ef274b857fbd466a
sio:SIO_000628
miriam-gene:4204
,
lld:C0235820
;
a
sio:SIO_001121
.
}
dgn-np:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_provenance
{
dgn-np:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_assertion
dcterms:description
"[The unmitigated impact of mutant MECP2 can be inferred from the few males who have been born into RTT kindreds with such severe neonatal encephalopathy that they did not survive their second year.]. 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:11180222
;
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:NP307448.RAq49eef8mW8tJY1oSQ9nA-nc9SEwLoLdYw-m0xGS9tM0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:05+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" .
}