Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_assertion> ?p ?o ?g. }
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- NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_assertion type Assertion NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_head.
- NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_assertion wasGeneratedBy ECO_0000203 NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_provenance.
- NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_assertion wasDerivedFrom befree-2016 NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_provenance.
- NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_assertion SIO_000772 11257260 NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_provenance.
- NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_assertion evidence source_evidence_literature NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_provenance.
- NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_assertion description "[A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311448.RAnl7NfJRmwmMBmL0T0CJHMF6a9QmpJkdKHL8YZdRuwkI130_provenance.