Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_assertion> ?p ?o ?g. }
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- NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_assertion type Assertion NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_head.
- NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_assertion description "[These results demonstrate the importance of ACVRL1 and ENG mutations in German hereditary hemorrhagic telangiectasia (HHT) patients displaying mutation frequencies over 80%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_provenance.
- NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_assertion evidence source_evidence_literature NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_provenance.
- NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_assertion SIO_000772 15880681 NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_provenance.
- NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_assertion wasDerivedFrom lhgdn-20090331 NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_provenance.
- NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_assertion wasGeneratedBy ECO_0000203 NP210757.RAcLs7t0XvsiGw_04yiuk2xmSFHXp9EeBmN29-USdINII130_provenance.