Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance.
- NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_assertion description "[Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance.
- NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_assertion evidence source_evidence_curated NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance.
- NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_assertion SIO_000772 23603762 NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance.
- NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_assertion wasDerivedFrom uniprot-20150221 NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance.
- NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_assertion wasGeneratedBy ECO_0000218 NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP21.RAFZW5GdfpY2d0x2sPg-Gr0oedWmIAkHXnI3eSxUsfH1c130_provenance.