@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE
> .
@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:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_head
{
this:
np:hasAssertion
dgn-np:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_assertion
;
np:hasProvenance
dgn-np:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_provenance
;
np:hasPublicationInfo
dgn-np:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_assertion
a
np:Assertion
.
dgn-np:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_provenance
a
np:Provenance
.
dgn-np:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_assertion
{
miriam-gene:7337
a
ncit:C16612
.
lld:C0032897
a
ncit:C7057
.
dgn-gda:DGN97af9eae49ca0a10c7f08c481999ebfe
sio:SIO_000628
miriam-gene:7337
,
lld:C0032897
;
a
sio:SIO_001121
.
}
dgn-np:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_provenance
{
dgn-np:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_assertion
dcterms:description
"[The results from this study show (a) two additional copies of proximal 15q loci, D15S9 through D15S12, in mentally retarded patients with an inv dup(15) but without AS or PWS and (b) no additional copies of these loci in patients with a normal phenotype or with PWS.]. 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:7942854
;
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:NP303990.RALk_y79b8_Ux2B5ZU_S6--uXYGKoaeb-aMxBCAJCZipE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:54+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: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" .
}