Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_assertion> ?p ?o ?g. }
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- NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_assertion type Assertion NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_head.
- NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_assertion description "[Mutations in PRG4 cause the autosomal recessive, human disorder camptodactyly-arthropathy-coxa vara-pericarditis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_provenance.
- NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_assertion evidence source_evidence_literature NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_provenance.
- NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_assertion SIO_000772 16000300 NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_provenance.
- NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_assertion wasDerivedFrom befree-20140225 NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_provenance.
- NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_assertion wasGeneratedBy ECO_0000203 NP420439.RAD8Fng-kOMmHgoWQwQcQLjEGMIzcqUe8zv4gzeUzb1es130_provenance.