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- source_evidence_literature type ECO_0000212 NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_provenance.
- NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_assertion description "[These results suggest that clinical manifestations in SHOC2 mutation-positive patients partially overlap with those in patients with typical Noonan or CFC syndrome and show that easily pluckable/loose anagen hair is distinctive in SHOC2 mutation-positive patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_provenance.
- NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_assertion evidence source_evidence_literature NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_provenance.
- NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_assertion SIO_000772 20882035 NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_provenance.
- NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_assertion wasDerivedFrom befree-2016 NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_provenance.
- NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_assertion wasGeneratedBy ECO_0000203 NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_provenance.
- befree-2016 importedOn "2016-02-19" NP842734.RAc1hAzpsfiHoO6aIZ4XD5x_zxEE1kTfUqx5GyH1kTrYY130_provenance.