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- source_evidence_literature type ECO_0000212 NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance.
- NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_assertion description "[Our findings expand the number of large FBN1 deletions, and emphasize the importance of screening for large genomic deletions in connective tissue disorders featuring aortopathies, especially for those with classic Marfan phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance.
- NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_assertion evidence source_evidence_literature NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance.
- NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_assertion SIO_000772 21936929 NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance.
- NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_assertion wasDerivedFrom befree-2016 NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance.
- NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_assertion wasGeneratedBy ECO_0000203 NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance.
- befree-2016 importedOn "2016-02-19" NP925412.RAOzSLx3oCsMsRL2KRU8dpvbUYOJPquIF20privwDzE60130_provenance.