Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance.
- NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_assertion description "[We therefore screened the WAS gene in 14 young SCN males with wild-type ELA2 and identified 2 with novel mutations, one who presented with myelodysplasia (Ile294Thr) and the other with classic SCN (Ser270Pro).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance.
- NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_assertion evidence source_evidence_literature NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance.
- NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_assertion SIO_000772 16804117 NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance.
- NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_assertion wasDerivedFrom befree-20140225 NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance.
- NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_assertion wasGeneratedBy ECO_0000203 NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP634864.RAe_YWWbwMB3Wbzl_L21Pgp7LL113MiHvbcvg7Tsk0qD8130_provenance.