Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.
- NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_assertion description "[We report here that mutations of LRTOMT are associated with profound nonsyndromic hearing loss at the DFNB63 locus on human chromosome 11q13.3-q13.4.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.
- NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_assertion evidence source_evidence_curated NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.
- NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_assertion SIO_000772 18953341 NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.
- NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_assertion wasDerivedFrom uniprot-20150221 NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.
- NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_assertion wasGeneratedBy ECO_0000218 NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP4223.RAW3-_8mdzq-rZ9smRHf5Iz_crDPP2Mqk-VnxBFlL46QI130_provenance.