Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance.
- NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_assertion description "[Other features noted in this kindred including epilepsy, cognitive impairment, depression, and migraine did not segregate with the HSP phenotype or mutation, and therefore the significance of these features to SPG4 is unclear.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance.
- NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_assertion evidence source_evidence_literature NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance.
- NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_assertion SIO_000772 15667412 NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance.
- NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_assertion wasDerivedFrom befree-20140225 NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance.
- NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_assertion wasGeneratedBy ECO_0000203 NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP471577.RAsvyxQT1lLo18SEtYoyZ4ACL6Qm8p_CeV6tv1MnD9U9k130_provenance.