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- NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_assertion type Assertion NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_head.
- NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_assertion description "[The conclusion that most variants of OI are caused by mutations in the structural genes for type I procollagen has broad implications for other diseases that affect connective tissue, diseases such as chondrodystrophies, osteoarthritis, and osteoporosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_provenance.
- NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_assertion evidence source_evidence_literature NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_provenance.
- NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_assertion SIO_000772 2683782 NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_provenance.
- NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_assertion wasDerivedFrom befree-20140225 NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_provenance.
- NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_assertion wasGeneratedBy ECO_0000203 NP196091.RAV_1XmsiG5_WB10GZi3L_h1v-PQa75p0dwx2zYmyY50k130_provenance.