Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_assertion type Assertion NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_head.
- NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_assertion description "[This study demonstrates evidence of a novel locus SPG38 for Silver syndrome (SS) and suggests that genetic defects in SPG4 might lead to broad clinical features overlapped with those of SS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance.
- NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_assertion evidence source_evidence_literature NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance.
- NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_assertion SIO_000772 18401025 NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance.
- NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_assertion wasDerivedFrom befree-20140225 NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance.
- NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_assertion wasGeneratedBy ECO_0000203 NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance.