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- NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_assertion type Assertion NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_head.
- NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_assertion wasGeneratedBy ECO_0000218 NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_provenance.
- NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_assertion wasDerivedFrom uniprot-20130724 NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_provenance.
- NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_assertion SIO_000772 21949523 NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_provenance.
- NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_assertion evidence source_evidence_curated NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_provenance.
- NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_assertion description "[A sporadic case of Loeys-Dietz syndrome type I with two novel mutations of the TGFBR2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6545.RAcRTB0FIbaXzIX-gTX3v59CpZvlbahSj_6xJmizj0lQQ130_provenance.