Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP636235.RASpOXtndBN2UXwr22sfd7rc0UAnmWiU_RlozMbQslku8130_provenance.