@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o
> .
@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:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_head
{
this:
np:hasAssertion
dgn-np:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_assertion
;
np:hasProvenance
dgn-np:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_provenance
;
np:hasPublicationInfo
dgn-np:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_assertion
a
np:Assertion
.
dgn-np:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_provenance
a
np:Provenance
.
dgn-np:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_assertion
{
miriam-gene:8091
a
ncit:C16612
.
lld:C0206650
a
ncit:C7057
.
dgn-gda:DGN32f6604c44448731955cd6ea00dc16e0
sio:SIO_000628
miriam-gene:8091
,
lld:C0206650
;
a
sio:SIO_001121
.
}
dgn-np:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_provenance
{
dgn-np:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_assertion
dcterms:description
"[Benign mesenchymal neoplasms associated with rearrangements of the DNA architectural factor gene HMGIC on chromosome 12 include lipomas, uterine leiomyomata, pulmonary chondroid hamartomas, endometrial polyps, salivary gland pleomorphic adenomas, and breast fibroadenomas.]. 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:11550285
;
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:NP587691.RA6rTlcV5yWidSmO1fNJ15azLr1Eh3wsbaQDDE93IEg5o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}