Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_assertion> ?p ?o ?g. }
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- NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_assertion type Assertion NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_head.
- NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_assertion wasGeneratedBy ECO_0000203 NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_provenance.
- NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_assertion wasDerivedFrom lhgdn-20090331 NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_provenance.
- NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_assertion SIO_000772 17056636 NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_provenance.
- NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_assertion evidence source_evidence_literature NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_provenance.
- NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_assertion description "[Noonan syndrome affected individuals show heterozygous PTPN11 mutations ]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP123484.RAHahbF9LVL2qNrtFO4dKDiaqpvdkX6Jw2Pmpy413Urpk130_provenance.