Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance.
- NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_assertion description "[Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance.
- NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_assertion evidence source_evidence_literature NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance.
- NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_assertion SIO_000772 19167195 NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance.
- NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_assertion wasDerivedFrom befree-2016 NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance.
- NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_assertion wasGeneratedBy ECO_0000203 NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance.
- befree-2016 importedOn "2016-02-19" NP716253.RAY821wQnqDMMF-JFmqIpb3h0hxgLIoG3EOIP0g1pCoGg130_provenance.