Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP446348.RAnX93uSn1ondzXfyy9xVu7WNRtSRsWUX95IpOqdGs-Ec130_provenance.