Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance.
- NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_assertion description "[Our results suggest that mutations in BIN1 cause centronuclear myopathy by interfering with remodeling of T tubules and/or endocytic membranes, and that the functional interaction between BIN1 and DNM2 is necessary for normal muscle function and positioning of nuclei.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance.
- NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_assertion evidence source_evidence_curated NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance.
- NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_assertion SIO_000772 17676042 NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance.
- NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_assertion wasDerivedFrom ctd_human-20150221 NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance.
- NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_assertion wasGeneratedBy ECO_0000218 NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP8403.RANFdqp21jPNFVKgM69q08OVoA8qif-9SvZ8UfGaqcqcI130_provenance.