Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion> ?p ?o ?g. }
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- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion type Assertion NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_head.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion description "[Here, we report on germline mutations of PHOX2B in both a familial case of NB and a patient with the HSCR-NB association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion evidence source_evidence_literature NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion SIO_000772 15024693 NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion wasDerivedFrom befree-2016 NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.
- NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_assertion wasGeneratedBy ECO_0000203 NP435799.RAHLOSS79I65ClOBTcJLC1EgqqZNCQWHwCDlOYu1SqOMg130_provenance.