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- source_evidence_literature type ECO_0000212 NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_provenance.
- NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_assertion description "[Based on the previous finding that mutations in COL3A1 cause type IV EDS, our study indicates a possible common pathological pathway linking connective tissue diseases and brain malformations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_provenance.
- NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_assertion evidence source_evidence_literature NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_provenance.
- NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_assertion SIO_000772 22235340 NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_provenance.
- NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_assertion wasDerivedFrom befree-2016 NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_provenance.
- NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_assertion wasGeneratedBy ECO_0000203 NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_provenance.
- befree-2016 importedOn "2016-02-19" NP952381.RAE4EgMd-ebnNkuh6r8gDSTwPyoudiP0vYdER3TKXei40130_provenance.