Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance.
- NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_assertion description "[Mutations in ALDH1A3 represent a frequent cause of microphthalmia/anophthalmia in consanguineous families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance.
- NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_assertion evidence source_evidence_curated NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance.
- NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_assertion SIO_000772 24777706 NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance.
- NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_assertion wasDerivedFrom uniprot-20150221 NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance.
- NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_assertion wasGeneratedBy ECO_0000218 NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP2661.RAKmqWEgl6mgD5Ed0JUPK367y9evNTG11_xNBZbe17I9c130_provenance.