Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_assertion> ?p ?o ?g. }
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- NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_assertion type Assertion NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_head.
- NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_assertion wasGeneratedBy ECO_0000218 NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_provenance.
- NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_assertion wasDerivedFrom uniprot-2016 NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_provenance.
- NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_assertion SIO_000772 10406984 NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_provenance.
- NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_assertion evidence source_evidence_curated NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_provenance.
- NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_assertion description "[Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP271.RABBl6oG9siFKuNxs68QJy-cbevAlqUSqJpuuxUKr6CJE130_provenance.