Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_assertion> ?p ?o ?g. }
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- NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_assertion type Assertion NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_head.
- NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_assertion description "[The infant was found to be heterozygous for the prothrombin G20210A mutation and homozygous for the methylenetetrahydrofolate reductase C667T mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_provenance.
- NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_assertion evidence source_evidence_literature NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_provenance.
- NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_assertion SIO_000772 13679943 NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_provenance.
- NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_assertion wasDerivedFrom befree-20150227 NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_provenance.
- NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_assertion wasGeneratedBy ECO_0000203 NP576323.RA84gLsph4NrHqNdyH-RrTeoFGCzU77Awj8RvvkNzsZxU130_provenance.