Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP343568.RA8a-uIfWTBLFlnxOV2SNDXvvNRxBeA9AbxilJ1oLN_1g130_provenance.