Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_assertion> ?p ?o ?g. }
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- NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_assertion type Assertion NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_head.
- NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_assertion description "[The segregation of polymorphic alleles at and around loci for p75NGFR, TRKA, TRKB, BDNF, and familial dysautonomia (another hereditary sensory neuropathy having features in common with HSN II) virtually excluded these genes as the cause of HSN II in this family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_provenance.
- NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_assertion evidence source_evidence_literature NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_provenance.
- NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_assertion SIO_000772 8895241 NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_provenance.
- NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_assertion wasDerivedFrom befree-20150227 NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_provenance.
- NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_assertion wasGeneratedBy ECO_0000203 NP1002883.RANJ0qsnyidYmIFu1t_KpRidnjuZ3xKxBkEQbBa6HMZ9A130_provenance.