Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance.
- NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_assertion description "[Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenita.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance.
- NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_assertion evidence source_evidence_curated NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance.
- NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_assertion SIO_000772 11748852 NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance.
- NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_assertion wasDerivedFrom uniprot-20150221 NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance.
- NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_assertion wasGeneratedBy ECO_0000218 NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance.
- uniprot-20150221 importedOn "2015-02-21" NP2886.RAkHUFkK1RtcaZaZ8Xj46YA2UI8r1ko90-hOIwFACaCc4130_provenance.