Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_assertion> ?p ?o ?g. }
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- NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_assertion type Assertion NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_head.
- NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_assertion description "[Huntington?s disease (HD) is a neurodegenerative disorder caused by a mutation in the HTT gene (mHTT) encoding the protein huntingtin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_provenance.
- NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_assertion evidence source_evidence_literature NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_provenance.
- NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_assertion SIO_000772 25732261 NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_provenance.
- NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_assertion wasDerivedFrom befree-2016 NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_provenance.
- NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_assertion wasGeneratedBy ECO_0000203 NP1267544.RAS8Xtc2kF4WBFWD9kJhi2JZQtxi9e_znj2ANkN_L6Wyk130_provenance.