Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_assertion> ?p ?o ?g. }
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- NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_assertion type Assertion NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_head.
- NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_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." NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_provenance.
- NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_assertion evidence source_evidence_literature NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_provenance.
- NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_assertion SIO_000772 15024693 NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_provenance.
- NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_assertion wasDerivedFrom befree-2016 NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_provenance.
- NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_assertion wasGeneratedBy ECO_0000203 NP435797.RA1xjSQCu2wgc9rPMB1Zi2bq7nDrcEKRvqqIQulHItEho130_provenance.