@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg
> .
@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:NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg130_head
{
this:
np:hasAssertion
dgn-np:NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg130_assertion
a
np:Assertion
.
dgn-np:NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg130_provenance
a
np:Provenance
.
dgn-np:NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:4204
a
ncit:C16612
.
lld:C0235820
a
ncit:C7057
.
dgn-gda:DGN2df6a93e5e04b0b8f04ec8871f672fda
sio:SIO_000628
miriam-gene:4204
,
lld:C0235820
;
a
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.
}
dgn-np:NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg130_provenance
{
dgn-np:NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg130_assertion
dcterms:description
"[In this study, DNA samples from individuals with schizophrenia and other psychiatric diseases were scanned in order to explore whether the phenotypic spectrum of mutations in the MECP2 gene can extend beyond the traditional diagnoses of RTT in females and severe neonatal encephalopathy in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:15211631
;
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:NP449244.RAg-ftEdTaiAPxwBo_PgoVYXNcQAg9x52DL4W39BtKTPg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:08+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
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" .
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pav:version
"v4.0.0" .
}