Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_assertion> ?p ?o ?g. }
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- NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_assertion type Assertion NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_head.
- NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_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." NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_provenance.
- NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_assertion evidence source_evidence_literature NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_provenance.
- NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_assertion SIO_000772 23456229 NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_provenance.
- NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_assertion wasDerivedFrom befree-20140225 NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_provenance.
- NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_assertion wasGeneratedBy ECO_0000203 NP860144.RAWfM9zSzXwqjCSXmqO9rDlKSoQRssk9NTgY8W2Ys_oKU130_provenance.