Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_assertion> ?p ?o ?g. }
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- NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_assertion type Assertion NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_head.
- NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_assertion wasGeneratedBy ECO_0000203 NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_provenance.
- NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_assertion wasDerivedFrom befree-20150227 NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_provenance.
- NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_assertion SIO_000772 21428921 NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_provenance.
- NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_assertion evidence source_evidence_literature NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_provenance.
- NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_assertion description "[Mutations in genes encoding either hamartin [TSC1 (tuberous sclerosis complex 1)] or tuberin (TSC2) result in a multisystem disorder characterized by the development of benign tumours and hamartomas in several organs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP760006.RAA3VFsz6XYnyGT5rPFCHnvBR7qAGycw7R1c3_dcc-h3Q130_provenance.