NP597281.RAbRtIBdhX Jp4ugyA- mm3lKhRCFk-1qGN5LfmLgz-uE
has assertion: NP597281.RAbRtIBdhX Jp4ugyA- mm3lKhRCFk-1qGN5LfmLgz-uE130 assertion
has provenance: NP597281.RAbRtIBdhX Jp4ugyA- mm3lKhRCFk-1qGN5LfmLgz-uE130 provenance
has publication info: NP597281.RAbRtIBdhX Jp4ugyA- mm3lKhRCFk-1qGN5LfmLgz-uE130 publicationInfo
type: Nanopublication
created: 2014-10-02T12:37:59+02:00
rights: http://opendatacommons.org/licenses/odbl/1.0/
rights holder: IBIGroup
subject: SIO_000983
used data: disgenetrdf
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: v2.1.0.0

NP597281.RAbRtIBdhX Jp4ugyA- mm3lKhRCFk-1qGN5LfmLgz-uE130 assertion
type: Assertion
description: [Several mutations within the gene coding for the cardiac beta myosin heavy chain (designed MYH7) have been shown to be responsible for Familial Hypertrophic Cardiomyopathy (FHC) in several families, and evidence of genetic heterogeneity has been reported.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/7815466
was generated by: ECO_0000203

befree-20140225
imported on: 2014-02-25

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

disgenetrdf
version: v2.1.0