@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_head
{
this:
np:hasAssertion
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_assertion
;
np:hasProvenance
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_provenance
;
np:hasPublicationInfo
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_assertion
a
np:Assertion
.
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_provenance
a
np:Provenance
.
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_assertion
{
miriam-gene:85358
a
ncit:C16612
.
lld:C1849930
a
ncit:C7057
.
dgn-gda:DGNb7a1769460664294e102f89c742ebb9b
sio:SIO_000628
miriam-gene:85358
,
lld:C1849930
;
a
sio:SIO_001121
.
}
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_provenance
{
dgn-np:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_assertion
dcterms:description
"[Although SHANK3 is considered to be the most likely candidate gene for the neurological abnormalities in PMDS patients, the cellular and molecular phenotypes associated with this syndrome in human neurons are unknown.]. 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:24132240
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP164140.RAOshA_Z8mXRwpZB-HAWegXQDDXFQW_3fsX-tVInOP5EY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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:disgenetrdf
;
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
"v2.1.0.0" .
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"v2.1.0" .
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