@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s
> .
@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:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_head
{
this:
np:hasAssertion
dgn-np:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_assertion
;
np:hasProvenance
dgn-np:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_provenance
;
np:hasPublicationInfo
dgn-np:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_assertion
a
np:Assertion
.
dgn-np:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_provenance
a
np:Provenance
.
dgn-np:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0023798
a
ncit:C7057
.
dgn-gda:DGNcf9d45014755ef9e71dfd748bf4d779a
sio:SIO_000628
miriam-gene:4221
,
lld:C0023798
;
a
sio:SIO_001121
.
}
dgn-np:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_provenance
{
dgn-np:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_assertion
dcterms:description
"[The discovery of mutations of the menin gene in a few multiple endocrine neoplasma type 1 (MEN I)-associated lipomas and loss of heterozygosity (LOH) on chromosome 11q13 in some sporadic lipomas has stimulated the hypothesis that lipomas may belong to the group of sporadic tumors caused by defects of the gene responsible for MEN I.]. 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:10741690
;
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:NP868511.RAhh8EcohRCxt9WmgNISTJCdHlupuaf8spZ8BnKeu_V-s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:50+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" .
}