Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance.
- NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_assertion description "[In a Portuguese population of 45 HCM patients, 5 (11.1%) had mutations in the MYBPC3 gene (3 missense mutations--theoretically less frequent in the MYBPC3 gene--and 2 deletions).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance.
- NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_assertion evidence source_evidence_literature NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance.
- NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_assertion SIO_000772 16566405 NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance.
- NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_assertion wasDerivedFrom gad-20150221 NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance.
- NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_assertion wasGeneratedBy ECO_0000203 NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP99656.RASi2p685G6XoixixpjcehiLYd3mCiV-hXujUGbAieGAA130_provenance.