Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance.
- NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_assertion description "[Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance.
- NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_assertion evidence source_evidence_literature NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance.
- NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_assertion SIO_000772 21221624 NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance.
- NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_assertion wasDerivedFrom befree-2016 NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance.
- NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_assertion wasGeneratedBy ECO_0000203 NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance.
- befree-2016 importedOn "2016-02-19" NP864422.RA_alZbcTZ4G2TmZGvi8VeEEeN-4UDaOzvIQRCDKSOgK4130_provenance.