Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.
- 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.
- uniprot-2016 importedOn "2016-01-25" NP7249.RAT9ywMyUIFvn_fLyC4Fm0TNt_K_qc7hLyHudUcCHH_Kw130_provenance.