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- source_evidence_literature type ECO_0000212 NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_provenance.
- NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_assertion description "[Mutations in the C-terminal half of MID1, an RBCC (RING, B-box and coiled-coil) protein, have recently been shown to underlie the X-linked form of OS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_provenance.
- NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_assertion evidence source_evidence_literature NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_provenance.
- NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_assertion SIO_000772 11030761 NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_provenance.
- NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_assertion wasDerivedFrom befree-20150227 NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_provenance.
- NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_assertion wasGeneratedBy ECO_0000203 NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP901820.RAGZZJdoINJjbZ7zS2X0TpyungMzIeeSlUtRt-a-40Soo130_provenance.