Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance.
- NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_assertion description "[CACNA1H mutations in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance.
- NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_assertion evidence source_evidence_curated NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance.
- NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_assertion SIO_000772 16754686 NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance.
- NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_assertion wasDerivedFrom ctd_human-20130708 NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance.
- NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_assertion wasGeneratedBy ECO_0000218 NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP10405.RAZvfWUWRwn_VbdQ2l6zjkCk19g0dZVFqu4Y5tsi1jJKk130_provenance.