Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_assertion> ?p ?o ?g. }
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- NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_assertion type Assertion NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_head.
- NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_assertion description "[Genetic defects of PMCA function produce disease phenotypes: the best characterized is a form of deafness in mice and in humans linked to PMCA2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_provenance.
- NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_assertion evidence source_evidence_literature NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_provenance.
- NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_assertion SIO_000772 23413890 NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_provenance.
- NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_assertion wasDerivedFrom befree-20140225 NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_provenance.
- NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_assertion wasGeneratedBy ECO_0000203 NP852087.RAntlVMsKtXqu-5pwtBZKZJ8QRcbmWnzrfRRqpZC6b_Qw130_provenance.