Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion> ?p ?o ?g. }
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- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion type Assertion NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_head.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion description "[The gene mutated in families displaying the `incomplete phenotype` of CSNB (i.e., CSNB2) has recently been identified.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion evidence source_evidence_literature NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion SIO_000772 10982042 NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion wasDerivedFrom befree-20140225 NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.
- NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_assertion wasGeneratedBy ECO_0000203 NP283617.RAeb-heSWKvYqGKomX5Gr7DmsIpBDWpL1fXfPXZHFCK6s130_provenance.