Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance.
- NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_assertion description "[A novel mutation in MIP associated with congenital nuclear cataract in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance.
- NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_assertion evidence source_evidence_curated NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance.
- NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_assertion SIO_000772 21245956 NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance.
- NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_assertion wasDerivedFrom uniprot-2016 NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance.
- NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_assertion wasGeneratedBy ECO_0000218 NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6492.RAImuYli0J9H9a1DHBQpSZg7p3enqr2_F3-G8_cAcfFNc130_provenance.