Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_assertion> ?p ?o ?g. }
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- NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_assertion type Assertion NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_head.
- NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_assertion description "[These new data and the finding of linkage to MID1 in the absence of a demonstrable open reading frame mutation in a further family support the conclusion that X-linked OS results from loss of function of MID1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_provenance.
- NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_assertion evidence source_evidence_literature NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_provenance.
- NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_assertion SIO_000772 11030761 NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_provenance.
- NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_assertion wasDerivedFrom befree-20140225 NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_provenance.
- NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_assertion wasGeneratedBy ECO_0000203 NP435383.RA3wlBDGi0PcDE-C48_nOUBIm6TMhVTG0Fjrn1nnBswz4130_provenance.