Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_assertion> ?p ?o ?g. }
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- NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_assertion type Assertion NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_head.
- NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_assertion description "[The X-linked recessive centronuclear/myotubular myopathy (XLR-CNM/MTM1), a severe neonatal disorder characterized by generalized hypotonia, muscle weakness and primary asphyxia, has recently been mapped to Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_provenance.
- NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_assertion evidence source_evidence_literature NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_provenance.
- NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_assertion SIO_000772 1822801 NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_provenance.
- NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_assertion wasDerivedFrom befree-20150227 NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_provenance.
- NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_assertion wasGeneratedBy ECO_0000203 NP576408.RA_Dtbh9XQ9Nlwu8RFbGwCPcamYKJ2blUKasN7M-nLACI130_provenance.