Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_assertion type Assertion NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_head.
- NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_assertion description "[Two common endoglin mutations in families with hereditary hemorrhagic telangiectasia in the Netherlands Antilles: evidence for a founder effect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_provenance.
- NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_assertion evidence source_evidence_curated NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_provenance.
- NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_assertion SIO_000772 10982033 NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_provenance.
- NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_assertion wasDerivedFrom uniprot-2016 NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_provenance.
- NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_assertion wasGeneratedBy ECO_0000218 NP1015.RAh8AtgmIDNxBYbtSLW9BNqUDqfOUc58fbm56n0ygTzDE130_provenance.