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- NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_assertion type Assertion NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_head.
- NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_assertion wasGeneratedBy ECO_0000203 NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_provenance.
- NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_assertion wasDerivedFrom befree-20150227 NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_provenance.
- NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_assertion SIO_000772 8807664 NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_provenance.
- NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_assertion evidence source_evidence_literature NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_provenance.
- NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_assertion description "[The identification of a gentic marker associated with significant alterations in enzyme activity will facilitate the analysis of a possible role for the COMT gene in neuropsychiatric conditions in which abnormalities in catecholamine neurotransmission are believed to occur, including mood disorders, schizophrenia, obsessive compulsive disorder, alcohol and substance abuse, and attention deficit hyperactivity disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322106.RAd2_0HTHyQ_nUyBzBFLvApoGf8CpKxt0hHyGCHMv1xM4130_provenance.