Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.
- NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.
- NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_assertion evidence source_evidence_literature NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.
- NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_assertion SIO_000772 23398611 NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.
- NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_assertion wasDerivedFrom befree-20150227 NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.
- NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_assertion wasGeneratedBy ECO_0000203 NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682492.RA15J37c9e2yadakhlQhMkQc9J_HuBJazi53BLsh1Nkos130_provenance.