@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM
> .
@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:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_head
{
this:
np:hasAssertion
dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_assertion
;
np:hasProvenance
dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_provenance
;
np:hasPublicationInfo
dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_assertion
a
np:Assertion
.
dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_provenance
a
np:Provenance
.
dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_assertion
{
miriam-gene:4842
a
ncit:C16612
.
lld:C0524528
a
ncit:C7057
.
dgn-gda:DGNf5b4aad5bd0520b5e1e19602a98f141d
sio:SIO_000628
miriam-gene:4842
,
lld:C0524528
;
a
sio:SIO_001121
.
}
dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_provenance
{
dgn-np:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_assertion
dcterms:description
"[Diagnostic assignments of AS based on three commonly used approaches have low agreement and lead to different results in comparisons of IQ profiles, patterns of comorbidity, and familial aggregation of psychiatric symptoms across the approach-specific resultant groups of HFA, AS, and PDD-NOS.]. 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:15909408
;
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:NP340900.RAV28s0FC2fk8IBtxZHGP48OYBNO1c1J__lwv8Be9OWAM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:20+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" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}