Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_assertion type Assertion NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_head.
- NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_assertion description "[C596G mutation in FBN1 causes Marfan syndrome with exotropia in a Chinese family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_provenance.
- NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_assertion evidence source_evidence_literature NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_provenance.
- NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_assertion SIO_000772 25729264 NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_provenance.
- NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_assertion wasDerivedFrom befree-2016 NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_provenance.
- NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_assertion wasGeneratedBy ECO_0000203 NP1267336.RAChZNa3Xz8tLSgX3H2Y_7n14bjr--SRSAbdhCHxHtxHE130_provenance.