Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_assertion> ?p ?o ?g. }
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- NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_assertion type Assertion NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_head.
- NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_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." NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_provenance.
- NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_assertion evidence source_evidence_literature NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_provenance.
- NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_assertion SIO_000772 19651702 NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_provenance.
- NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_assertion wasDerivedFrom befree-20140225 NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_provenance.
- NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_assertion wasGeneratedBy ECO_0000203 NP722922.RAOM0bLwfluluq8qBPpPBMwR0DUFibVerVn_azyIdvoJ4130_provenance.