Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_assertion> ?p ?o ?g. }
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- NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_assertion type Assertion NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_head.
- NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_assertion description "[Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_provenance.
- NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_assertion evidence source_evidence_curated NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_provenance.
- NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_assertion SIO_000772 25848753 NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_provenance.
- NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_assertion wasDerivedFrom ctd_human-2016 NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_provenance.
- NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_assertion wasGeneratedBy ECO_0000218 NP35376.RAbiM6rXmrz3KZh_aCQ44cdhnfaTz5jDLN6hnWZeibX2U130_provenance.