Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_assertion> ?p ?o ?g. }
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- NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_assertion type Assertion NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_head.
- NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_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." NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_provenance.
- NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_assertion evidence source_evidence_literature NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_provenance.
- NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_assertion SIO_000772 23456229 NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_provenance.
- NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_assertion wasDerivedFrom befree-20140225 NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_provenance.
- NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_assertion wasGeneratedBy ECO_0000203 NP321319.RAiz3kG4KFzm845tuyW-kkSaiUjuG-ahT7entvp6XKArw130_provenance.