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- source_evidence_literature type ECO_0000212 NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_provenance.
- NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_assertion description "[This study demonstrates evidence of a novel locus SPG38 for Silver syndrome (SS) and suggests that genetic defects in SPG4 might lead to broad clinical features overlapped with those of SS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_provenance.
- NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_assertion evidence source_evidence_literature NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_provenance.
- NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_assertion SIO_000772 18401025 NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_provenance.
- NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_assertion wasDerivedFrom befree-2016 NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_provenance.
- NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_assertion wasGeneratedBy ECO_0000203 NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_provenance.
- befree-2016 importedOn "2016-02-19" NP665034.RAgospQAyrXQ9J-WWdhxkQbUeECUl8QwgZLWcTKrdsVu4130_provenance.