Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_assertion> ?p ?o ?g. }
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- NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_assertion type Assertion NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_head.
- NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_assertion description "[Molecular analysis (FRET) was performed on selected cases for three common hereditary thrombophilias: mutations in factor V Leiden (FVL), prothrombin G20210A (PT), and methylenetetrahydrofolate reductase (MTHFR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_provenance.
- NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_assertion evidence source_evidence_literature NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_provenance.
- NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_assertion SIO_000772 15813553 NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_provenance.
- NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_assertion wasDerivedFrom befree-2016 NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_provenance.
- NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_assertion wasGeneratedBy ECO_0000203 NP488710.RA4HKtGd3P71NQiBDEDC0R1ZGQwaW9XB-TorEc5BvnpLo130_provenance.