Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion description "[HGPS (Hutchinson-Gilford progeria syndrome) is a rare genetic disease affecting children causing them to age and die prematurely.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion evidence source_evidence_literature NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion SIO_000772 20074076 NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion wasDerivedFrom befree-20150227 NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_assertion wasGeneratedBy ECO_0000203 NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP938305.RAB7tjWRs6vhj0W0Kp-FP-vxMOV05cTDcOL_OviS1GgVo130_provenance.