Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_assertion> ?p ?o ?g. }
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- NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_assertion type Assertion NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_head.
- NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_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." NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance.
- NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_assertion evidence source_evidence_literature NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance.
- NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_assertion SIO_000772 22560297 NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance.
- NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_assertion wasDerivedFrom befree-20140225 NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance.
- NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_assertion wasGeneratedBy ECO_0000203 NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance.