Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_assertion type Assertion NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_head.
- NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_assertion wasGeneratedBy ECO_0000203 NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_provenance.
- NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_assertion wasDerivedFrom befree-2016 NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_provenance.
- NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_assertion SIO_000772 2148653 NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_provenance.
- NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_assertion evidence source_evidence_literature NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_provenance.
- NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_assertion description "[In a group of 37 consecutive patients with arterial occlusive disease presenting before the age of 45, three patients were found heterozygous for hereditary protein S deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP886531.RAAiJH9p1j0xAuvl1RlwXkrSvKjdyzKqeRHPDkdYxBlsc130_provenance.