Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_assertion type Assertion NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_head.
- NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_assertion description "[This report describes a patient with thalassemia intermedia-like phenotype born to normal parents in whom globin gene sequencing detected a novel abnormal hemoglobin (Hb) due to a T to A substitution at codon 60 of the beta-globin gene arising as a de novo mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_provenance.
- NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_assertion evidence source_evidence_literature NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_provenance.
- NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_assertion SIO_000772 1985702 NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_provenance.
- NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_assertion wasDerivedFrom befree-2016 NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_provenance.
- NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_assertion wasGeneratedBy ECO_0000203 NP771713.RABXZAHFIB9drSH8vOPs5KAtOexo5o1ZO3Qvfcpz90lq0130_provenance.