Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance.
- NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_assertion description "[Most forms of OI result from point mutations in the genes (COL1A1 and COL1A2) that encode the chains of type I procollagen or mutations that affect the expression of these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance.
- NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_assertion evidence source_evidence_literature NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance.
- NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_assertion SIO_000772 2683783 NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance.
- NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_assertion wasDerivedFrom befree-2016 NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance.
- NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_assertion wasGeneratedBy ECO_0000203 NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1296076.RAlsFwWtrezKRkPXAIP9MA5RfOKG9XW1uRCG43xD-UuDo130_provenance.