Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance.
- NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_assertion description "[Characterization of SH2D1A missense mutations identified in X-linked lymphoproliferative disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance.
- NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_assertion evidence source_evidence_curated NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance.
- NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_assertion SIO_000772 11477068 NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance.
- NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_assertion wasDerivedFrom uniprot-2016 NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance.
- NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_assertion wasGeneratedBy ECO_0000218 NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP1553.RAgqBVaXbd3S12o_IQE0JfcHKJ7xO-jDAz6iuLtiz6bWc130_provenance.