Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_assertion> ?p ?o ?g. }
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- NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_assertion type Assertion NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_head.
- NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_provenance.
- NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_assertion evidence source_evidence_literature NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_provenance.
- NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_assertion SIO_000772 19651702 NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_provenance.
- NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_assertion wasDerivedFrom befree-2016 NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_provenance.
- NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_assertion wasGeneratedBy ECO_0000203 NP755131.RAU03kG1c8Tkpw4zA1siOSQr-UgBNUuW_3xh_BRADysP4130_provenance.