Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance.
- NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_assertion description "[Mutations in the ATR-X gene (ATRX) that encodes a putative global transcription factor have been identified in patients with ATR-X as well as those with other forms of X-linked mental retardation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance.
- NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_assertion evidence source_evidence_literature NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance.
- NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_assertion SIO_000772 10995512 NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance.
- NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_assertion wasDerivedFrom befree-20150227 NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance.
- NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_assertion wasGeneratedBy ECO_0000203 NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP990736.RA-mFSMTXPZKJWVaQnG6F0Hh2T63YKyqA-01mUEfJX5Tk130_provenance.