Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance.
- NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_assertion description "[A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance.
- NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_assertion evidence source_evidence_curated NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance.
- NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_assertion SIO_000772 10441344 NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance.
- NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_assertion wasDerivedFrom uniprot-20130724 NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance.
- NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_assertion wasGeneratedBy ECO_0000218 NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP6302.RAa4OMy2BZxXv4a21B3fZJLv0eeWMeebTxAB1yeUuA26U130_provenance.