Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_assertion> ?p ?o ?g. }
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- NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_assertion type Assertion NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_head.
- NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_assertion description "[The family's Brown syndrome trait was analyzed for linkage to the known congenital fibrosis syndrome loci and the CFEOM2 gene, ARIX, was sequenced in affected individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_provenance.
- NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_assertion evidence source_evidence_literature NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_provenance.
- NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_assertion SIO_000772 12324876 NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_provenance.
- NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_assertion wasDerivedFrom befree-20150227 NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_provenance.
- NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_assertion wasGeneratedBy ECO_0000203 NP252333.RAKGYkiL0zq3Qv5MkPqunD4SklORvOnbhgfvKFsIoqfDo130_provenance.