Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_assertion> ?p ?o ?g. }
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- NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_assertion type Assertion NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_head.
- NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_assertion description "[Therefore, the major cause underlying autosomal recessive NDI is the misrouting of AQP2 mutant proteins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance.
- NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_assertion evidence source_evidence_literature NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance.
- NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_assertion SIO_000772 9048343 NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance.
- NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_assertion wasDerivedFrom befree-2016 NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance.
- NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_assertion wasGeneratedBy ECO_0000203 NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance.