Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_assertion> ?p ?o ?g. }
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- NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_assertion type Assertion NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_head.
- NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_assertion description "[Mutations of the selenoprotein N gene (SEPN1) cause SEPN1-related myopathy (SEPN1-RM), a novel early-onset muscle disorder formerly divided into four different nosological categories.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_provenance.
- NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_assertion evidence source_evidence_literature NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_provenance.
- NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_assertion SIO_000772 19557870 NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_provenance.
- NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_assertion wasDerivedFrom befree-2016 NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_provenance.
- NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_assertion wasGeneratedBy ECO_0000203 NP747703.RAH8TgZSA1NFLWt7icqMpGTtdC56T_UgtIv0RYWoVPd70130_provenance.