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- source_evidence_literature type ECO_0000212 NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_provenance.
- NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_assertion description "[Molecular and cytogenetic analysis in two patients with microdeletions of 7p and Greig syndrome: hemizygosity for PGAM2 and TCRG genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_provenance.
- NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_assertion evidence source_evidence_literature NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_provenance.
- NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_assertion SIO_000772 1981052 NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_provenance.
- NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_assertion wasDerivedFrom befree-2016 NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_provenance.
- NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_assertion wasGeneratedBy ECO_0000203 NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_provenance.
- befree-2016 importedOn "2016-02-19" NP767956.RAha4wwSwptGmGr1TgRK3_DefPaJuPNfMJAbWNM9adih0130_provenance.