Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_assertion> ?p ?o ?g. }
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- NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_assertion type Assertion NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_head.
- NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_assertion description "[This indel mutation in FHL1 broadens the spectrum of FHL1-related disorders and implicates it in the pathogenesis of NS spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance.
- NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_assertion evidence source_evidence_literature NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance.
- NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_assertion SIO_000772 23456229 NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance.
- NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_assertion wasDerivedFrom befree-20150227 NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance.
- NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_assertion wasGeneratedBy ECO_0000203 NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance.