Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP431676.RAl8Xtn1GQWmC7Wf-0AHCrB3u_8oHz6drpATGYQ2pHYWE130_provenance.