http://rdf.disgenet.org/resource/nanopub/NP205081.RAQDaCzZ3vBtiwnAd--bGf-NkpUh-_4aoR7s_PZ-U9oD8
type: Nanopublication
created: 2016-05-13T12:43:19+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

http://rdf.disgenet.org/resource/nanopub/NP205081.RAQDaCzZ3vBtiwnAd--bGf-NkpUh-_4aoR7s_PZ-U9oD8130_assertion
type: Assertion
description: [in a study of 918 chromosomes for mutations leading to beta-thalassemia and sickle cell anemia in postnatal and prenatal cases, one new Hb variant and one new mutation, Cod 3 (+T) were found/abnormalities in fetuses were also documented.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
evidence: DisGeNET evidence - LITERATURE
SIO_000772: http://identifiers.org/pubmed/15153712
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