@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss
> .
@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:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_head
{
this:
np:hasAssertion
dgn-np:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_assertion
;
np:hasProvenance
dgn-np:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_provenance
;
np:hasPublicationInfo
dgn-np:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_assertion
a
np:Assertion
.
dgn-np:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_provenance
a
np:Provenance
.
dgn-np:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0035372
a
ncit:C7057
.
dgn-gda:DGN4a210c413291ac676040320885702cdd
sio:SIO_000628
miriam-gene:4204
,
lld:C0035372
;
a
sio:SIO_001121
.
}
dgn-np:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_provenance
{
dgn-np:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_assertion
dcterms:description
"[From these results, it is suggested that the clinical phenotype of RTT is variable and it is important to investigate the MECP2 genotype for patients having more than five criteria and not only in those who exhibit all RTT diagnostic criteria.]. 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:11376998
;
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:NP319087.RAN-fdgy1ZKeRgioukcAVXq8k9Yr3nHUsYacdC43mCTss130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:10+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" .
}