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- source_evidence_literature type ECO_0000212 NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_provenance.
- NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_assertion description "[HPTH has been associated with a number of familial diseases, such as multiple endocrine neoplasia-type 1 (MEN1), multiple endocrine neoplasia-type2A (MEN2A), neurofibromatosis type1 (NF1) and HPTH with multiple ossifying jaw fibromas (HPT-JT Syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_provenance.
- NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_assertion evidence source_evidence_literature NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_provenance.
- NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_assertion SIO_000772 16299679 NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_provenance.
- NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_assertion wasDerivedFrom befree-20140225 NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_provenance.
- NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_assertion wasGeneratedBy ECO_0000203 NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP465194.RAaWSf6xcjPcImfRO9Pv6Rl92cF_SvT-uqGkpyC_tFCHM130_provenance.