Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_assertion type Assertion NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_head.
- NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_assertion description "[Prenatal exclusion of Crouzon syndrome by mutation analysis of FGFR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_provenance.
- NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_assertion evidence source_evidence_literature NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_provenance.
- NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_assertion SIO_000772 15916101 NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_provenance.
- NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_assertion wasDerivedFrom befree-2016 NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_provenance.
- NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_assertion wasGeneratedBy ECO_0000203 NP496387.RAwIOpGKzVIOy0bITqM_yac7egOgYmwyUfB1u43UwGwVs130_provenance.