Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_assertion> ?p ?o ?g. }
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- NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_assertion type Assertion NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_head.
- NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.
- NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_assertion evidence source_evidence_curated NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.
- NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_assertion SIO_000772 23063620 NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.
- NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_assertion wasDerivedFrom uniprot-2016 NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.
- NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_assertion wasGeneratedBy ECO_0000218 NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.