@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I
> .
@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:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_head
{
this:
np:hasAssertion
dgn-np:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_assertion
;
np:hasProvenance
dgn-np:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_provenance
;
np:hasPublicationInfo
dgn-np:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_assertion
a
np:Assertion
.
dgn-np:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_provenance
a
np:Provenance
.
dgn-np:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0023798
a
ncit:C7057
.
dgn-gda:DGN9fd60cc7eb3f0acc8f29a1c376e2ebf0
sio:SIO_000628
miriam-gene:5728
,
lld:C0023798
;
a
sio:SIO_001121
.
}
dgn-np:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_provenance
{
dgn-np:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_assertion
dcterms:description
"[Hereditary predisposition to lipomas is observed in familial multiple lipomatosis (OMIM 151900) and benign cervical lipomatosis (OMIM 151800) and can also be associated with mutations in the MEN1 and PTEN genes (OMIM 131100 and 153480, respectively).]. 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:11571558
;
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:NP276796.RAkkV0DrKgbwoY4piYG28l5tdEooDVeUKB9wDdGcoRg4I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:35+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" .
}