NP243421.RA2-DG-hyj30zksuDy6 RWYQMY7 TunQSks v8V1tSIA
type: Nanopublication
has assertion: NP243421.RA2-DG-hyj30zksuDy6 RWYQMY7 TunQSks v8V1tSIA130 assertion
has provenance: NP243421.RA2-DG-hyj30zksuDy6 RWYQMY7 TunQSks v8V1tSIA130 provenance
has publication info: NP243421.RA2-DG-hyj30zksuDy6 RWYQMY7 TunQSks v8V1tSIA130 publicationInfo
created: 2016-05-13T12:43:36+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetv3.0rdf
authored by: http://orcid.org/0000-0001-5999-6269
authored by: http://orcid.org/0000-0002-7534-7661
authored by: 0000-0002-9383-528X
authored by: http://orcid.org/0000-0003-0169-8159
authored by: http://orcid.org/0000-0003-1244-7654
created by: http://orcid.org/0000-0003-0169-8159
version: v4.0.0.0

NP243421.RA2-DG-hyj30zksuDy6 RWYQMY7 TunQSks v8V1tSIA130 assertion
type: Assertion
description: [Although the familial occurrence of these rare tumors might be coincidental, it cannot be ruled out that, beside FH, mutations in another as yet unknown gene could give rise to both leiomyosarcoma and kidney cancer ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/18986479
was generated by: ECO_0000203

lhgdn-20090331
imported on: 2009-03-31

DisGeNET evidence - LITERATURE
type: ECO_0000212
comment: Gene-disease associations inferred from text-mining the literature.

disgenetv3.0rdf
version: v4.0.0