Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion wasGeneratedBy ECO_0000203 NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion wasDerivedFrom befree-20150227 NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion SIO_000772 22408652 NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion evidence source_evidence_literature NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.
- NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_assertion description "[Nearly all cases of FOP are caused by the identical mutation in the ACVR1 gene that causes a single amino acid substitution, R206H, in the bone morphogenetic protein (BMP) type I receptor ACVR1 (formerly known as ALK2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222202.RAvROEdEASLzcQuSP7J_tjvH-jWY0XfM_6Bv5R_tpbZVM130_provenance.