@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U
> .
@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:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_head
{
this:
np:hasAssertion
dgn-np:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_assertion
;
np:hasProvenance
dgn-np:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_provenance
;
np:hasPublicationInfo
dgn-np:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_assertion
a
np:Assertion
.
dgn-np:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_provenance
a
np:Provenance
.
dgn-np:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_assertion
{
miriam-gene:4204
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN5c1a164ead62549b64a4f4fdf71bcaca
sio:SIO_000628
miriam-gene:4204
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_provenance
{
dgn-np:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_assertion
dcterms:description
"[In this study, the question was addressed as to whether implementation of systematic screening of MECP2 in patients with an unexplained mental retardation in DNA diagnostics would be reasonable, and the spectrum of phenotypes resulting from mutations in this gene was further explored.]. 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:14560307
;
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:NP416994.RAMZ_gFUH9geUeFYV0YAya9FZ3CYpn2cKBPZIIMIKdv1U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:54+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" .
}