Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion wasGeneratedBy ECO_0000203 NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion wasDerivedFrom befree-20150227 NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion SIO_000772 22152678 NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion evidence source_evidence_literature NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.
- NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_assertion description "[Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP526816.RA38DUQZY3l0s1_kyfDNZ6-R1r900oIZ4sz5Xh_cT2lVM130_provenance.