Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP1368167.RAi7qXlFHkSFy310S1oPq13aFjniokoUtzWqf48zp1Q_4130_provenance.