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- NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_assertion type Assertion NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_head.
- NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_assertion description "[Congenital asplenia in mice and humans with mutations in a Pbx/Nkx2-5/p15 module.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_provenance.
- NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_assertion evidence source_evidence_literature NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_provenance.
- NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_assertion SIO_000772 22560297 NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_provenance.
- NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_assertion wasDerivedFrom befree-20140225 NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_provenance.
- NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_assertion wasGeneratedBy ECO_0000203 NP906358.RAGS98jHukCCkJpKxUS6rIducacoiCcarxVnIP0WADsTc130_provenance.