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- source_evidence_literature type ECO_0000212 NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_provenance.
- NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_assertion description "[We have identified six different point mutations in the HCS gene in nine patients with MCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_provenance.
- NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_assertion evidence source_evidence_literature NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_provenance.
- NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_assertion SIO_000772 8817339 NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_provenance.
- NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_assertion wasDerivedFrom befree-20150227 NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_provenance.
- NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_assertion wasGeneratedBy ECO_0000203 NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP459131.RAYO7wtItCwzQKhfHNIf86Fu0Q2TK1uV63C88Ym6b9Bf4130_provenance.