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- source_evidence_literature type ECO_0000212 NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_provenance.
- NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_assertion description "[Loss of function of paraplegin (encoded by the SPG7 gene) causes hereditary spastic paraplegia, a disease characterized by retrograde degeneration of cortical motor axons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_provenance.
- NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_assertion evidence source_evidence_literature NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_provenance.
- NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_assertion SIO_000772 19289403 NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_provenance.
- NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_assertion wasDerivedFrom befree-20150227 NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_provenance.
- NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_assertion wasGeneratedBy ECO_0000203 NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710151.RAiQ5a2Jtkf7CP82cI8QHsJ2mspdwFbhPBe1T_ILJI5HM130_provenance.