Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance.
- NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_assertion description "[A mutation in the B-box region of TRIM32 has also been shown to result in a more pleiotropic disorder, Bardet-Biedl Syndrome (BBS11).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance.
- NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_assertion evidence source_evidence_literature NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance.
- NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_assertion SIO_000772 21496629 NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance.
- NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_assertion wasDerivedFrom befree-2016 NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance.
- NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_assertion wasGeneratedBy ECO_0000203 NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance.
- befree-2016 importedOn "2016-02-19" NP887429.RAVgQRXGyTViJ8Q0XvFy3zqGjEQscUorTQwwt4mtdKR_8130_provenance.