Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance.
- NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_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." NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance.
- NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_assertion evidence source_evidence_literature NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance.
- NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_assertion SIO_000772 16299679 NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance.
- NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_assertion wasDerivedFrom befree-20140225 NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance.
- NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_assertion wasGeneratedBy ECO_0000203 NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP917693.RAIfTETrcKtxyN0_RU8Ph8viMExUnpAKleoPI5u_1JVGc130_provenance.