Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance.
- NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_assertion wasGeneratedBy ECO_0000203 NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance.
- NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_assertion wasDerivedFrom befree-20140225 NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance.
- NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_assertion SIO_000772 9027848 NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance.
- NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_assertion evidence source_evidence_literature NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance.
- NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_assertion description "[Merosin-deficient congenital muscular dystrophy (CMD) is caused by mutations in the laminin alpha 2 chain gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP459204.RAqRSauwAh1m6P83bT0PkEfpjlD9ezoVLPp1Pzjv3IMVg130_provenance.