Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance.
- NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_assertion description "[None of the GSD Ia HCA had biallelic mutations in the HNF1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance.
- NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_assertion evidence source_evidence_literature NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance.
- NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_assertion SIO_000772 19762333 NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance.
- NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_assertion wasDerivedFrom befree-20140225 NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance.
- NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_assertion wasGeneratedBy ECO_0000203 NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP339957.RABb7rIhvrQE9bMHti06CVaBpoKMCaPS-fSgo1UfkHK1g130_provenance.