Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_assertion> ?p ?o ?g. }
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- NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_assertion type Assertion NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_head.
- NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_provenance.
- NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_assertion evidence source_evidence_literature NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_provenance.
- NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_assertion SIO_000772 11030761 NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_provenance.
- NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_assertion wasDerivedFrom befree-2016 NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_provenance.
- NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_assertion wasGeneratedBy ECO_0000203 NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_provenance.