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- NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_assertion type Assertion NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_head.
- NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_assertion description "[Mutations in ALK1, a TGF-beta type 1 receptor, previously known to cause type 2 hereditary haemorrhagic telangiectasia (HHT), have also been reported in a few HHT families with clinical and histological features of PPH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.
- NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_assertion evidence source_evidence_literature NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.
- NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_assertion SIO_000772 11817654 NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.
- NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_assertion wasDerivedFrom befree-2016 NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.
- NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_assertion wasGeneratedBy ECO_0000203 NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.