Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance.
- NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_assertion description "[A number of autosomal-dominant genes have been described that primarily cause ALS or FTLD such as progranulin (GRN), valosin-containing protein (VCP), and TAR DNA-Binding Protein (TARDBP), and for each of these conditions there are a small number of cases with both ALS and FTLD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance.
- NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_assertion evidence source_evidence_literature NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance.
- NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_assertion SIO_000772 22477152 NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance.
- NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_assertion wasDerivedFrom befree-20140225 NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance.
- NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_assertion wasGeneratedBy ECO_0000203 NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP427127.RANOqQIL_21QNiU8Pyud8GYna_cbUOeV1ebXjp4vbxFpg130_provenance.