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- source_evidence_literature type ECO_0000212 NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_provenance.
- NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_assertion description "[Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet-Biedl syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_provenance.
- NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_assertion evidence source_evidence_literature NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_provenance.
- NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_assertion SIO_000772 23219996 NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_provenance.
- NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_assertion wasDerivedFrom befree-2016 NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_provenance.
- NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_assertion wasGeneratedBy ECO_0000203 NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_provenance.
- befree-2016 importedOn "2016-02-19" NP1034065.RASi6u4C_HXclM93xFyyJiCNGridSwU4Jwi0qHlq1BrHI130_provenance.