@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ
> .
@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:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_head
{
this:
np:hasAssertion
dgn-np:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_assertion
;
np:hasProvenance
dgn-np:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_assertion
a
np:Assertion
.
dgn-np:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_provenance
a
np:Provenance
.
dgn-np:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_assertion
{
miriam-gene:801
a
ncit:C16612
.
lld:C0751674
a
ncit:C7057
.
dgn-gda:DGNa6f9963ebde2a50ae4a1d91360b4b215
sio:SIO_000628
miriam-gene:801
,
lld:C0751674
;
a
sio:SIO_001121
.
}
dgn-np:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_provenance
{
dgn-np:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_assertion
dcterms:description
"[Deletion mutagenesis studies further suggested that this CaM binding domain is required for tuberin modulation of steroid receptor function and that mutations in this region may be involved in the pathology of TSC and LAM.]. 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:11811958
;
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:NP361944.RAHgkzED4i8u2xy46eN2tECT0mhrdGv5hz2cV9iUefalQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:32+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" .
}