Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.
- NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_assertion wasGeneratedBy ECO_0000203 NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.
- NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_assertion wasDerivedFrom befree-20150227 NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.
- NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_assertion SIO_000772 18989701 NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.
- NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_assertion evidence source_evidence_literature NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.
- NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_assertion description "[Mutations in MECP2 cause classic or preserved speech variant Rett syndrome and intellectual disability in females and early demise or marked neurodevelopmental handicap in males.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552197.RANmS42UVDKWjfSn2sAqNU1w08CHk0TT0o_U2iu0ZLEdc130_provenance.