Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance.
- NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_assertion description "[DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance.
- NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_assertion evidence source_evidence_curated NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance.
- NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_assertion SIO_000772 23504663 NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance.
- NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_assertion wasDerivedFrom uniprot-2016 NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance.
- NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_assertion wasGeneratedBy ECO_0000218 NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7405.RAnonUUTYm2T10jD5WrWHaCm_mLwz1NVTATVPaU74eV1Q130_provenance.