Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP696450.RASnQ4Ss7vJcCyBtLw-QakSD2HkiPDfVPRxKUjugPMi50130_provenance.