Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_assertion> ?p ?o ?g. }
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- NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_assertion type Assertion NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_head.
- NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_assertion description "[MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance.
- NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_assertion evidence source_evidence_literature NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance.
- NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_assertion SIO_000772 17427193 NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance.
- NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_assertion wasDerivedFrom befree-20150227 NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance.
- NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_assertion wasGeneratedBy ECO_0000203 NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance.