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- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion type Assertion NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_head.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion description "[L1 syndrome and X-linked NDI are distinct clinical disorders caused by mutations in the L1CAM and AVPR2 genes, respectively, located in adjacent positions in Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion evidence source_evidence_literature NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion SIO_000772 18553546 NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion wasDerivedFrom befree-20150227 NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion wasGeneratedBy ECO_0000203 NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.