@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w
> .
@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:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_head
{
this:
np:hasAssertion
dgn-np:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_assertion
;
np:hasProvenance
dgn-np:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_provenance
;
np:hasPublicationInfo
dgn-np:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_assertion
a
np:Assertion
.
dgn-np:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_provenance
a
np:Provenance
.
dgn-np:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0206658
a
ncit:C7057
.
dgn-gda:DGN9b9d385f682c47986966c454ee253440
sio:SIO_000628
miriam-gene:4221
,
lld:C0206658
;
a
sio:SIO_001121
.
}
dgn-np:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_provenance
{
dgn-np:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_assertion
dcterms:description
"[To test whether the MEN1 gene is involved in the pathogenesis of multiple smooth muscle tumors, we examined the 11q13 loss of heterozygosity (LOH) and clonality patterns in 15 leiomyomata of the esophagus, lung, and uterus from five patients with MEN1.]. 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:11549605
;
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:NP531299.RAHhCIR2D6kSYTZ8uvERMgISlQAuKJt1lA0Mp-mqrXj0w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}