Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_assertion> ?p ?o ?g. }
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- NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_assertion type Assertion NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_head.
- NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_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." NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_provenance.
- NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_assertion evidence source_evidence_literature NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_provenance.
- NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_assertion SIO_000772 22560297 NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_provenance.
- NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_assertion wasDerivedFrom befree-20140225 NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_provenance.
- NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_assertion wasGeneratedBy ECO_0000203 NP911865.RANHSalkaInC64Hdf1XqQB2_V69SAld5GuQwEMDCCpT0w130_provenance.