Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance.
- NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_assertion description "[Since RET function in mouse spermatogonial stem cells has been extensively studied, we are able to suggest that the MEN2B mutation provides a selective advantage by altering the PI3K/AKT and SFK signaling pathways.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance.
- NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_assertion evidence source_evidence_literature NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance.
- NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_assertion SIO_000772 22359510 NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance.
- NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_assertion wasDerivedFrom befree-20150227 NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance.
- NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_assertion wasGeneratedBy ECO_0000203 NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP232135.RAlSA49CoFxYQ9r1-PlM6x7nTX65zWm_vXvTguWtkc4bc130_provenance.